Greiner Bio-One North America, Inc. - VACUETTE 5 ml CAT Serum Clot Activator - Class 2 Recall
VACUETTE TUBE 5 mL CAT Serum Separator Clot Activator, Item Number: 456018P - Product Usage: are used to collect, transport, and process blood for testing serum, plasma or whole blood in the clinical laboratory. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 30, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - FlexLab (different names by distributors: Accelerator a3600 and Aptio Automation) - Class 2 Recall
Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual robot) FLX-290-10; FLX-290-20 and Track to Rack Module FLX-295-10- Intended Clinical Chemistry Test Systems - Product Usage: The FlexLab 3.6 Automation is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The system consolidates analytical instruments, such as the ARCHITECT c8000 System into a unified workstation that perform a variety of instrument specific assays such as Sodium, Potassium and Chloride. Sodium, Potassium and Chloride measur...
Source: Medical Device Recalls - September 17, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - FlexLab (different names by distributors: Accelerator a3600 and Aptio Automation) - Class 2 Recall
Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual robot) FLX-290-10; FLX-290-20 and Track to Rack Module FLX-295-10- Intended Clinical Chemistry Test Systems - Product Usage: The FlexLab 3.6 Automation is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The system consolidates analytical instruments, such as the ARCHITECT c8000 System into a unified workstation that perform a variety of instrument specific assays such as Sodium, Potassium and Chloride. Sodium, Potassium and Chloride measur...
Source: Medical Device Recalls - September 17, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - FlexLab (with different names by distributors: Accelerator a3600 and Aptio Automation) - Class 2 Recall
FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot) FLX-290-10; FLX-290-20 and Track to Rack Module FLX-295-10- Intended Laboratory Automation system - Product Usage: The FlexLab 3.6 Automation is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The system consolidates analytical instruments, such as the ARCHITECT c8000 System into a unified workstation that perform a variety of instrument specific assays such as Sodium, Potassium and Chloride. Sodium, Potassium and Chloride measurements are use...
Source: Medical Device Recalls - September 17, 2020 Category: Medical Devices Source Type: alerts

Siemens Healthcare Diagnostics Inc - epoc BGEM Test Card - Class 2 Recall
Siemens epoc BGEM Test Card-In vitro diagnostic device for the quantitative testing of samples of heparinized or un-anticoagulated arterial, venous or capillary whole blood in the laboratory or at the point of care SMN#/Model #: 10736382 (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 16, 2020 Category: Medical Devices Source Type: alerts

Ortho Clinical Diagnostics - VITROS AntiSARSCoV2 IgG Reagent Pack - Class 2 Recall
VITROS Anti-SARS-CoV-2 IgG Reagent Pack, COV2IgG, VITROS CoV2G. Catalog number 6199919, UDI 10758750033355 - Product Usage: Rx ONLY. For in vitro diagnostic and Laboratory Professional use. For emergency authorization use only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 8, 2020 Category: Medical Devices Source Type: alerts

Ortho Clinical Diagnostics - VITROS AntiSARSCoV2 Total Reagent - Class 2 Recall
VITROS Anti-SARS-CoV-2 Total Reagent, COV2TOT, VITROS CoV2T. Catalog number 6199922, UDI 10758750033386 - Product Usage: Rx ONLY. For in vitro diagnostic and Laboratory Professional use. For emergency authorization use only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 8, 2020 Category: Medical Devices Source Type: alerts

Radiometer Medical ApS - ABL 80 COOX SYSTEM - Class 2 Recall
ABL80-FLEX CO-OX 393-841 Box Label, REF 393-841, IVD, CE, UDI: 05700693938417 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 30, 2020 Category: Medical Devices Source Type: alerts

Siemens Healthcare Diagnostics Inc. - Class 2 Recall
Siemens IMMULITE 2000 Immunoassay System - In vitro Chemistry Analyzer SMN #10380062 - Product Usage: are intended for professional use in a laboratory environment only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 30, 2020 Category: Medical Devices Source Type: alerts

Siemens Healthcare Diagnostics Inc. - Class 2 Recall
Siemens IMMULITE 2000 XPi Immunoassay System - In vitro Chemistry Analyzer SMN #10373214 - Product Usage: are intended for professional use in a laboratory environment only. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 30, 2020 Category: Medical Devices Source Type: alerts

Radiometer Medical ApS - ABL80 FLEX ANALYZER - Class 2 Recall
ABL80-FLEX-393-839 Box Label, REF 393-839, IVD, CE, UDI: 05700693938394 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 30, 2020 Category: Medical Devices Source Type: alerts

Siemens Healthcare Diagnostics, Inc. - CentraLink Data Management System and Atellica Data Manager (CentraLink/Atellica DM) - Class 2 Recall
(1) CentraLink Data Management System software version 16.0.2 Siemens Material Number (SMN): 11313246 (2) CentraLink Data Management System software version 16.0.3 Siemens Material Number (SMN): 11314337 Product Usage: are clinical laboratory information modules which consolidate test orders and test results, provide test ordering and priority routing information to automation, apply rules to test orders and auto-verification rules for test results, and provide integrated management of quality control of test system. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 27, 2020 Category: Medical Devices Source Type: alerts

Siemens Healthcare Diagnostics, Inc. - CentraLink Data Management System and Atellica Data Manager (CentraLink/Atellica DM) - Class 2 Recall
(1) Atellica Data Manager software version 1.0 Siemens Material Number (SMN): 11314237 (2) Atellica Data Manager software version 1.1 Siemens Material Number (SMN): 11316888 Product Usage: are clinical laboratory information modules which consolidate test orders and test results, provide test ordering and priority routing information to automation, apply rules to test orders and auto-verification rules for test results, and provide integrated management of quality control of test system. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 27, 2020 Category: Medical Devices Source Type: alerts

Abbott Laboratories - Accelerator APS Aliquoter Module - Class 2 Recall
Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system designed to automate sample handling and processing in the clinical laboratory. The system allows consolidations of multiple clinical chemistry and immunoassay analytical instruments into a unified workstation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 4, 2020 Category: Medical Devices Source Type: alerts

Radiometer Medical ApS - ABL90 FLEX PLUS - Class 2 Recall
ABL90 FLEX PLUS, model no. 393-02; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 29, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - Aptio Automation System - Class 2 Recall
Aptio Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00) - Product Usage: is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 29, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - FlexLab Automation System - Class 2 Recall
FlexLab Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00)is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 29, 2020 Category: Medical Devices Source Type: alerts

Radiometer Medical ApS - ABL90 FLEX - Class 2 Recall
ABL90 FLEX, model no. 393-090; and Spare Part Hemolyzer Units (902-980): R0526 - R0941 - Product Usage: are intended for use by trained technologists, nurses, physicians and therapists. It is intended for use in a laboratory environment, near patient or point-of-care setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 29, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - Accelerator a3600 Automation System - Class 2 Recall
Accelerator a3600 Automation System with Advia2120LAS Interface Module (P/N FLX-219-00, FLX-219-10), ImmunoCAP 1000 Interface Module (P/N FLX-226-01, FLX-226-10), or StaRRsed Interface Module (P/N FLX-268-00) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 29, 2020 Category: Medical Devices Source Type: alerts

Thermo Fisher Scientific (Monterrey) - Samco BioTite Sterile Specimen Container - Class 2 Recall
Samco Bio-Tite Sterile Specimen Container, 120mL/53mm, Bio-Tite Blue Cap Catalog Number: 07 0006 The specimen containers are used for temporary collection, transfer, and/or storage of body fluids and solid specimen samples for the purpose of laboratory testing. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 27, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - Accelerator a3600 Automation System - Class 2 Recall
Accelerator a3600 Automation System used with the following Modules: High Volume Storage(P/N FLX-270, FLX-271, FLX-276, FLX-282, FLX-283), HSQ Interface Module (P/N FLX-274), Aliquoter Module (P/N FLX-209), Rack Output Module ROM400 (P/N FLX-289), XN-9000 Interface Module (P/N FLX-290), Advia 2120 LAS Interface Module (P/N FLX-219), Vertical Transportation Module (P/N FLX -204), Rack Input Module (P/N FLX-214), AUWi System Interface Module (P/N FLX-286), Track To Rack Interface Module (P/N FLX-295) - Product Usage: is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in or...
Source: Medical Device Recalls - May 27, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - FlexLab (aka Accelerator a3600 and Aptio Automation) - Class 2 Recall
FlexLab Automation System used with the following Modules: High Volume Storage(P/N FLX-270, FLX-271, FLX-276, FLX-282, FLX-283), HSQ Interface Module (P/N FLX-274), Aliquoter Module (P/N FLX-209), Rack Output Module ROM400 (P/N FLX-289), XN-9000 Interface Module (P/N FLX-290), Advia 2120 LAS Interface Module (P/N FLX-219), Vertical Transportation Module (P/N FLX -204), Rack Input Module (P/N FLX-214), AUWi System Interface Module (P/N FLX-286), Track To Rack Interface Module (P/N FLX-295) - Product Usage: is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to aut...
Source: Medical Device Recalls - May 27, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - Inpeco SA - Class 2 Recall
Abbott Accelerator a3600, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: ACP-208-00 - Product Usage: The FlexLab (aka Accelerator a3600) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 15, 2020 Category: Medical Devices Source Type: alerts

Inpeco S.A. - Inpeco SA - Class 2 Recall
Inpeco FlexLab, ARCHITECT cSystem c8000/c16000 Interface Module, Part Numbers: FLX-208-00, FLX-208-10 - Product Usage: The FlexLab (aka Accelerator a3600) is a modular system designed to automate Pre-Analytical and Post-Analytical processing, sample handling in order to automate sample processing in the Laboratory. The systems consolidate multiple Analytical instruments into a unified workstation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 15, 2020 Category: Medical Devices Source Type: alerts

Radiometer Medical ApS - ABL90 FLEX - Class 2 Recall
ABL90 FLEX Analyzer, Model Numbers 393-090, with software versions below 3.4MR2 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 23, 2020 Category: Medical Devices Source Type: alerts

Radiometer Medical ApS - ABL 90 FLEX PLUS - Class 2 Recall
ABL90 FLEX PLUS Analyzer, Model Number 393-092 - Product Usage: It is intended for use in a laboratory environment, near patient or point-of-care setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 23, 2020 Category: Medical Devices Source Type: alerts

Beckman Coulter Inc. - LabPro Data Management System - Class 2 Recall
LabPro Data Management System, UDI: 15099590676872 - Product Usage: The LabPro Data Management System is a Microsoft Windows based software program and is intended to manage both microbial identification (ID) and antimicrobial agent susceptibility testing (AST) data generated from MicroScan instruments or manually entered microbiology test results, for use by trained laboratory personnel. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 7, 2020 Category: Medical Devices Source Type: alerts

Greiner Bio-One North America, Inc. - VACUETTE TUBE - Class 2 Recall
VACUETTE TUBE, 3.5mL CAL Serum Sep Clot Activator, REF 454067P - Product Usage: VACUETTE Tubes, Holders, and Needles are use together as a system for the collection of venous blood. VACUETTE tubes are used to collect, transport, and process blood for testing serum, plasma, or whole blood in the clinical laboratory. (Source: Medical Device Recalls)
Source: Medical Device Recalls - January 18, 2020 Category: Medical Devices Source Type: alerts

The Binding Site Group, Ltd. - Optilite CReactive Protein Kit - Class 2 Recall
Optilite C-Reactive Protein Kit - Product Usage: The Optilite C-Reactive Protein Reagent is intended for the quantitative in vitro determination of C-reactive protein (CRP) concentration in serum using the Binding Site Optilite analyser. Measurement of C-Reactive Protein aids in evaluation of the amount of injury to body tissues and for evaluation of infection, tissue injury, and inflammatory disorders. This test should be used in conjunction with other laboratory and clinical findings. The Optilite C-Reactive Protein Calibrator is intended for the calibration of the Optilite C-Reactive Protein Reagent on the Optilite anal...
Source: Medical Device Recalls - December 13, 2019 Category: Medical Devices Source Type: alerts

Randox Laboratories Ltd. - Rheumatoid Factor Calibrators - Class 2 Recall
Rheumatoid Factor Standard (RF CAL) Catalogue Number: RF2301 GTIN: 05055273205039 Product Usage: The Randox Rheumatoid Factor Latex-Enhanced Immunorutbidimetric Test Kit is an in vitro diagnostic reagent for the quantitative determination of rheumatoid factors (RF) in human serum. This test kit may be used to facilitate the detection and diagnosis of Rheumatoid Arthritis. RF have also been observed in the serum of patients with systemic lupus eruthematosus, hepatitis. Liver cirrhosis and syphilis. However, in these conditions the RF titre is much lower than in rheumatoid arthritis. This test kit must be used by suitably qu...
Source: Medical Device Recalls - November 5, 2019 Category: Medical Devices Source Type: alerts

CooperSurgical, Inc. - RI Witness Embryology Heated Plate - Class 3 Recall
Embryology Heated Plate within the RI Witness, Model Numbers 6-70-807, 6-70-807-A, & 6-70-807-B - Product Usage: RI Witness uses Radio Frequency Identification (RFID) to detect and monitor all activity in the IVF laboratory. The system helps mitigate the risk of human error every time samples are moved from one dish or tube to another, and safeguards every step of the IVF cycle. While the heated plates comprise a heated composite surface with window for a light source. The heated plates comprise a heated composite surface with window for a light source and either sit on top of existing bench-tops or can be integrated t...
Source: Medical Device Recalls - October 3, 2019 Category: Medical Devices Source Type: alerts

Siemens Healthcare Diagnostics, Inc - Atellica IM antiCCP IgG (aCCP) Assay - Class 2 Recall
Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998 (100 Test) Test Version1.0 - Product Usage: The ADVIA Centaur¿ Anti-CCP IgG (aCCP) assay is for in vitro diagnostic use in the semi-quantitative determination of the IgG class of autoantibodies specific to cyclic citrullinated peptide (CCP) in human serum and plasma (K2-EDTA, lithium heparin) using the ADVIA Centaur XP system. Detection of anti-CCP antibodies is used as an aid in the diagnosis of rheumatoid arthritis (RA) and should be used in conjunction with other clinical information. Autoantibody levels represent one parameter in a multi-cri...
Source: Medical Device Recalls - September 27, 2019 Category: Medical Devices Source Type: alerts

House Of Spices (India) Issues Recall of " MDH Sambar Masala " Due To Salmonella Contamination
House of Spices (India) is recalling different lots of “MDH SAMBAR MASALA”, 3.5oz (100g) UPC code 6291103750327. This product is produced by R-PURE AGRO SPECIALITIES and distributed by HOUSE OF SPICES (INDIA). This product was tested by FDA through a certified laboratory to be positive for Salmonell (Source: FDA Food Safety)
Source: FDA Food Safety - September 9, 2019 Category: Food Science Authors: FDA Source Type: alerts

House Of Spices (india) Issues Recall of "MDH Sambar Masala" Due To Salmonella Contamination
House of Spices (India) is recalling different lots of “MDH SAMBAR MASALA”, 3.5oz (100g) UPC code 6291103750327. This product is produced by R-PURE AGRO SPECIALITIES and distributed by HOUSE OF SPICES (INDIA). This product was tested by FDA through a certified laboratory to be positive for Salmonell (Source: FDA Food Safety)
Source: FDA Food Safety - September 7, 2019 Category: Food Science Authors: FDA Source Type: alerts

Instrumentation Laboratory Co. - ROTEM extem (for use on ROTEM delta instrument) - Class 2 Recall
ROTEM ex-tem; US Part No: 503-05-US (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 7, 2019 Category: Medical Devices Source Type: alerts

Instrumentation Laboratory Co. - ROTEM extem (for use on ROTEM delta instrument) - Class 2 Recall
ROTEM ex-tem Rest of the world part No: 503-05 (ROW) (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 7, 2019 Category: Medical Devices Source Type: alerts

Instrumentation Laboratory Co. - ROTEM extem (for use on ROTEM delta instrument) - Class 2 Recall
ROTEM ex-tem Canada Part No: 503-05-CA (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 7, 2019 Category: Medical Devices Source Type: alerts

Hycor Biomedical Inc - Autostat II Rheumatoid Factor IgM ELISA - Class 2 Recall
AUTOSTAT II IgM Rheumatoid Factor, IVD, Part: FGA 05 Product Usage: Rheumatoid Factor IgM ELISA is intended to be utilized as either a manual or an automated procedure The Intended Use is as follows: Enzyme-linked immunosorbent assay method for the semi-quantitative determination of specific IgM Rheumatoid Factor antibodies in human serum. The results of the IgM RF assay can be used as an aid in the diagnosis of Rheumatoid Arthritis when supported by other laboratory and clinical investigations. Levels of these autoantibodies are one indicator in a multi-factorial diagnostic regime. The assay can be used with the HYCOR HyT...
Source: Medical Device Recalls - July 31, 2019 Category: Medical Devices Source Type: alerts

Phadia Ab - EliA RF IgM Immunoassay - Class 2 Recall
EliA RF IgM Well, REF 14-5600-01 Product Usage: Usage: EliA RF IgM is intended for the in vitro quantitative measurement of IgM class rheumatoid factor antibodies in human serum and plasma (Li-heparin and EDTA) to aid in the diagnosis of rheumatoid arthritis in conjunction with other laboratory and clinical findings. EliA RF IgM uses the EliA IgM method on the instrument Phadia 100, Phadia 250, Phadia 2500 and Phadia 5000. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 2, 2019 Category: Medical Devices Source Type: alerts

Tecan US, Inc. - Freedom EVO2 - Class 2 Recall
Freedom EVO 200 - Product Usage: It is intended for routine laboratory tasks, such as general purpose pipetting and general purpose liquid handling and robotic processes. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 21, 2019 Category: Medical Devices Source Type: alerts

Bio-Rad Laboratories, Inc - MRSASelect - Class 2 Recall
MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with other laboratory tests and clinical data available to aid in the identification and diagnosis of MRSA from patients with skin and soft-tissue infections. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 7, 2019 Category: Medical Devices Source Type: alerts

Bio-Rad Laboratories, Inc - MRSASelect II - Class 2 Recall
MRSASelect II, IVD, REF 63758 (20 plates per package). The MRSASelect is indicated for use in conjunction with other laboratory tests and clinical data available to aid in the identification and diagnosis of MRSA from patients with skin and soft-tissue infections. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 7, 2019 Category: Medical Devices Source Type: alerts

Abbott Laboratories - Multichem S Plus Level 1 - Class 3 Recall
Technopath Multichem S Plus Level 1 - Product Usage: Multichem S Plus (Assayed) is intended for use as an assayed quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the package insert. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 17, 2019 Category: Medical Devices Source Type: alerts

Abbott Laboratories - Multichem S Plus Level 2 - Class 3 Recall
Technopath Multichem S Plus Level 2 - Product Usage: Multichem S Plus (Assayed) is intended for use as an assayed quality control serum to monitor the precision of laboratory testing procedures for the analytes listed in the package insert. (Source: Medical Device Recalls)
Source: Medical Device Recalls - May 17, 2019 Category: Medical Devices Source Type: alerts

LIGHTNING PAIN RELIEF (Menthol) Cream [Clinical Resolution Laboratory, Inc.]
Updated Date: May 16, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 16, 2019 Category: Drugs & Pharmacology Source Type: alerts

NUMB520 (Lidocaine Hydrochloride, Phenylephrine Hydrochloride) Spray [Clinical Resolution Laboratory, Inc.]
Updated Date: May 16, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 16, 2019 Category: Drugs & Pharmacology Source Type: alerts

DR. LIGHTENING ULTRA-POTENT FACIAL (Hydroquinone) Cream [Clinical Resolution Laboratory, Inc.]
Updated Date: May 3, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - May 3, 2019 Category: Drugs & Pharmacology Source Type: alerts

Siemens Healthcare Diagnostics, Inc. - syngo Lab Data Manager System - Class 2 Recall
syngo Lab Data Manager System - Product Usage: syngo Lab Data Manager is a clinical system that assists medical laboratory professions with pre-analytic and post-analytic functions. It works in conjunction with multiple instruments, the laboratory information system (LIS) and the Siemens Healthcare Diagnostics Data Center. It supports the Siemens analyzers through delivery of applications and connectivity features. (Source: Medical Device Recalls)
Source: Medical Device Recalls - April 19, 2019 Category: Medical Devices Source Type: alerts

DR. LIGHTENING ULTRA-POTENT FACIAL CLEANSER (Hydroquinone) Cream [Clinical Resolution Laboratory, Inc.]
Updated Date: Apr 3, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - April 3, 2019 Category: Drugs & Pharmacology Source Type: alerts

Abbott Laboratories - CELLDYN Emerald - Class 2 Recall
CELL-DYN Emerald analyzer, REF 09H39-01. The CELL-DYN Emerald is an automated hematology analyzer intended for in-vitro diagnostic use in the clinical laboratory. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 30, 2019 Category: Medical Devices Source Type: alerts