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

Becton Dickinson & Co. - BD Synapsys Microbiology Informatics Solution - Class 2 Recall
BD Synapsys Laboratory Solutions Catalog Number:444150 Product Usage: BD Synapsys is a laboratory software solution providing data management and workflow management functionality across clinical diagnostic activities. The software integrates operational and clinical data points from laboratory hardware, with patient data received from external software systems allowing for the aggregation, evaluation, dissemination of knowledge using all data, anywhere, anytime. Currently Release 2 of BD Synapsys can connect to both Lab Automation (Kiestra) and BACTEC instruments. (Source: Medical Device Recalls)
Source: Medical Device Recalls - March 24, 2019 Category: Medical Devices Source Type: alerts

ZN7 DERM (Zinc Gluconate) Spray [Addison Biological Laboratory, Inc.]
Updated Date: Mar 20, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - March 20, 2019 Category: Drugs & Pharmacology Source Type: alerts

OCUFRESH (Water) Liquid [Optics Laboratory, Inc]
Updated Date: Feb 25, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 25, 2019 Category: Drugs & Pharmacology Source Type: alerts

MINIDROPS (Lubricant Eye Drops) Liquid [Optics Laboratory, Inc]
Updated Date: Feb 25, 2019 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - February 25, 2019 Category: Drugs & Pharmacology Source Type: alerts

Roche Diagnostics Corporation - Elecsys Anti HAV IgM - Class 2 Recall
Anti-HAV IgM test System, Material No. 11820591160 Product Usage: The Roche Elecsys Anti-HAV IgM immunoassay is used for the in vitro qualitative detection of IgM antibodies to hepatitis A virus (anti-HAV IgM) in human serum and plasma (potassium EDTA, lithium or sodium heparin, sodium citrate). The assay is intended for use as an aid in the laboratory diagnosis of an acute or recently acquired hepatitis A virus infection. Assay results, in conjunction with other laboratory results and clinical information, may be used to provide presumptive evidence of infection with hepatitis A virus in persons with signs and symptoms of...
Source: Medical Device Recalls - January 30, 2019 Category: Medical Devices Source Type: alerts

ORTHO-CLINICAL DIAGNOSTICS - VITROS HBeAg Reagent - Class 2 Recall
VITROS HBeAg Reagent, Cat. No 6801819 Product Usage: For the in vitro qualitative detection of hepatitis B e antigen (HBeAg) in human adult and pediatric (2 to 21 years old) serum from individuals who have symptoms of hepatitis or who may be at risk for hepatitis B virus (HBV) infection using the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System. Test results, in conjunction with other serological and clinical information, may be used for the laboratory diagnosis of individuals with acute or chronic hepatitis B, or recovery from hepatitis B infection. Th...
Source: Medical Device Recalls - January 4, 2019 Category: Medical Devices Source Type: alerts

OCCUFRESH (Water) Liquid [Optics Laboratory, Inc]
Updated Date: Dec 18, 2018 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - December 18, 2018 Category: Drugs & Pharmacology Source Type: alerts

Tosoh Bioscience Inc - Hemoglobin A1c Control - Class 3 Recall
Hemoglobin A1c Control, Part no. 220232 for use as quality control material to monitor the precision of laboratory testing procedures for HbA1c quantitation. (Source: Medical Device Recalls)
Source: Medical Device Recalls - December 14, 2018 Category: Medical Devices Source Type: alerts

GE Healthcare Biosciences - DeltaVision OMX SR Imaging System - Class 2 Recall
DeltaVision OMX SR Imaging System Model Number: 29115476 The DeltaVision OMX SR Imaging System is a piece of laboratory equipment for super resolution imaging offluorescently-la beling biological samples. Techniques such as 3D Structured Illumination, Total Internal Reflection Fluorescence and localization microscopy may be used to examine a variety of samples over long periods of time. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 21, 2018 Category: Medical Devices Source Type: alerts

Beckman Coulter Inc. - SortingDrive Product Part, SortingDrive Plus Kit (Sorting Drive Software v4.2.1) - Class 3 Recall
Sorting-Drive Product Part, Sorting-Drive Plus Kit (Sorting Drive Software v4.2.1), Part No. A89483, Beckman Coulter, Inc. The Sorting-Drive Plus Kit includes the Sorting-Drive 4.2.1 User Kit which includes the Sorting-Drive 4.2.1 Software DVD. . The Sorting-Drive software facilitates the Laboratory Information System (LIS) connection to AutoMate 2500 Family systems. . (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 1, 2018 Category: Medical Devices Source Type: alerts

Beckman Coulter Inc. - SortingDrive Professional Part, SortingDrive Professional Kit, (Sorting Drive Software v4.2.1) - Class 3 Recall
Sorting-Drive Professional Part, Sorting-Drive Professional Kit, (Sorting Drive Software v4.2.1), Part No. A94144, Beckman Coulter, Inc. The Sorting-Drive Professional Kit (PN A94144) includes the Sorting-Drive 4.2.1 User Kit (PN B95347) which includes the Sorting-Drive 4.2.1 Software DVD (PN B95346). This software version includes an option for manual barcode printing for sample tubes. Sorting-Drive software facilitates the Laboratory Information System (LIS) connection to AutoMate 2500 Family systems. (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 1, 2018 Category: Medical Devices Source Type: alerts

Acumedia Manufacturers, Inc. - Palcam Agar Base, Acumedia - Class 3 Recall
Palcam Agar Base, Acumedia, PN 7669, Product Usage - Dehydrated culture media used with supplements as a selective and differential medium for the detection and isolation of Listeria monocytogenes from foods and environmental samples in a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 27, 2018 Category: Medical Devices Source Type: alerts

Acumedia Manufacturers, Inc. - Campylobacter Blood Free Selective Medium - Class 3 Recall
Campylobacter Blood Free Selective Medium, PN 7527A Used with cefoperazone for the selective isolation of Campylobacter spp. In a laboratory setting. Not intended for use in the diagnosis of disease or other conditions in humans. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 27, 2018 Category: Medical Devices Source Type: alerts

Data Innovations, LLC - IM Abbott Alinity ciseries (abdicqii) accessory driver - Class 2 Recall
IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software product that can receive information from a hospital computer system (also called a Laboratory Information System [LIS]). (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 23, 2018 Category: Medical Devices Source Type: alerts

Hologic, Inc - Tomcat Instrument - Class 2 Recall
Tomcat Instrument, REF ASY-07379, Hologic Incorporated, automated laboratory sample processing instrument. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 12, 2018 Category: Medical Devices Source Type: alerts

Instrumentation Laboratory Co. - HemosIL ReadiPlasTin - Class 2 Recall
Hemosll ReadiPlasTin (10 mL Size), Part Number 0020301300 - Product Usage - HemosIL¿ ReadiPlasTin is an in vitro diagnostic thromboplastin reagent, based on recombinant human tissue factor, for the quantitative determination, in human citrated plasma, of Prothrombin Time (PT) and Fibrinogen, on the ACL TOP¿ Family of analyzers. The product is intended to be used for the evaluation of the extrinsic coagulation pathway and the monitoring of Oral Vitamin K Antagonist Therapy. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 6, 2018 Category: Medical Devices Source Type: alerts

Leica Microsystems, Inc. - HistoCare SPECTRA ST Stainer - Class 2 Recall
Leica Biosystems HistoCore SPECTRA ST, Slide Stainer, Automated Product Usage: The intended use of this device is a stainer for laboratory applications and intended for the preparation of histological and cytological specimens. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 4, 2018 Category: Medical Devices Source Type: alerts

Radiometer America Inc - The ABL90 FLEX Analyzer - Class 2 Recall
ABL90 FLEX analyzers with software versions 3.3MR1 or below. The ABL90 FLEX Analyzer is a portable, automated Analyzer that measures pH, blood gases, electrolytes, glucose, lactate, bilirubin and oximetry in whole blood. It is intended for use in a laboratory environment, near patient or point-of-care setting. (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 2, 2018 Category: Medical Devices Source Type: alerts

Biocare Medical, LLC - URO3 Triple Stain (CD44 p52 CK20) - Class 2 Recall
URO-3 Triple Stain (CD44 + p53) with CK20, Catalog #: PM370TSAA, Package Type: Bag, which contains components: a) CD44 + p53, Catalog #: PM373DSAA, Package Type: Bottle, and b) CK20, Catalog #: PM062AA, Package Type: Bottle Product Usage: URO-3 Triple Stain (CD44 + p53) with CK20 is a cocktail of mouse monoclonal and rabbit monoclonal antibodies that is intended for laboratory use in the qualitative identification of CD44, p53 and CK20 proteins by immunohistochemistry (IHC) in formalin-fixed paraffin-embedded (FFPE) human tissues, primarily for bladder cancer characterization. The clinical interpretation of any staining or...
Source: Medical Device Recalls - September 20, 2018 Category: Medical Devices Source Type: alerts

Ventana Medical Systems Inc - iView DAB Detection Kit w/o Secondary Antibody - Class 1 Recall
iView DAB Detection Kit w/o Secondary Antibody, Catalog Number 05266173001, Model 760-093. For laboratory use. (Source: Medical Device Recalls)
Source: Medical Device Recalls - September 15, 2018 Category: Medical Devices Source Type: alerts

Stanbio Laboratory, LP - Power adapter for the HemoPoint H2 meter, Model G3000 series - Class 2 Recall
Stanbio AC power adapter for the HemoPoint H2 meter, Model G3000 series. The firm name on the label for the HemoPoint H2 shows Manufactured by EKF-diagnostic GmbH, Germany. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 25, 2018 Category: Medical Devices Source Type: alerts

Roche Diagnostics Hematology - cobas m 511 integrated hematology analyzer - Class 2 Recall
cobas m 511 integrated hematology analyzer, Model Number 07261691190 Product Usage: The cobas m 511 integrated hematology analyzer is a quantitative, automated analyzer with cell locating capability. It is intended for in vitro diagnostic use by a skilled operator in the clinical laboratory. The system prepares a stained microscope slide from EDTA anticoagulated whole blood. It utilizes computer imaging to count the formed elements of blood and provide an image-based assessment of cell morphology, which may be reviewed by the operator, and also allows for manual classification of unclassified cells. The instrument reports ...
Source: Medical Device Recalls - July 27, 2018 Category: Medical Devices Source Type: alerts

Clarity Diagnostics Llc - Clarity Urocheck 10SG Urinalysis Strips - Class 3 Recall
Clarity Urocheck 10SG Urinalysis Strips, Model # DTG-10SG Product Usage: Clarity 10SG Urinalysis Reagent Strips (Urine) are for the qualitative and semi-quantitative detection of the following analytes in urine: Glucose, Bilirubin, Ketone (Acetoacetic acid), Specific Gravity, Blood, pH, Protein, Urobilinogen, Nitrite and Leukocytes. The Clarity Urinalysis Reagent Strips (Urine) are for single use in professional near-patient (point-of-care) and centralized laboratory locations, and are intended for professional use only. The strips are intended for use in screening at-risk patients to assist diagnosis in the following area...
Source: Medical Device Recalls - July 25, 2018 Category: Medical Devices Source Type: alerts

Immuno-Mycologics, Inc - Cryptococcal Antigen Lateral Flow Assay (CrAg LFA) - Class 2 Recall
Cryptococcal Antigen Lateral Flow Assay (CrAg LFA), Model # CR2003 Product Usage: The CrAg Lateral Flow Assay is an immunochromatographic test system for the qualitative or semi-quantitative detection of the capsular polysaccharide antigens of Cryptococcus species complex (Cryptococcus neoformans and Cryptococcus gattii) in serum and cerebral spinal fluid (CSF). The CrAg Lateral Flow Assay is a prescription-use laboratory assay which can aid in the diagnosis of cryptococcosis. (Source: Medical Device Recalls)
Source: Medical Device Recalls - July 11, 2018 Category: Medical Devices Source Type: alerts

Becton Dickinson & Company - BD Vacutainer Plus Plastic Citrate Blood Collection Tubes (Catalog Reference 366560) - Class 2 Recall
The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is an evacuated blood collection tube that provides a means of collecting, transporting, and processing blood in a closed tube. The buffered sodium citrate additive provides an anticoagulated specimen that may be used for clinical laboratory coagulation assays. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 21, 2018 Category: Medical Devices Source Type: alerts

Becton Dickinson & Company - BD Vacutainer Plus Plastic Citrate Blood Collection Tube - Class 2 Recall
The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is an evacuated blood collection tube that provides a means of collecting, transporting, and processing blood in a closed tube. The buffered sodium citrate additive provides an anticoagulated specimen that may be used for clinical laboratory coagulation assays. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 21, 2018 Category: Medical Devices Source Type: alerts

Becton Dickinson & Company - BD Vacutainer Plus Plastic Citrate Blood Collection Tube (Catalog Reference 364305) - Class 2 Recall
The BD Vacutainer Plus Plastic Citrate Blood Collection Tube is an evacuated blood collection tube that provides a means of collecting, transporting, and processing blood in a closed tube. The buffered sodium citrate additive provides an anticoagulated specimen that may be used for clinical laboratory coagulation assays. (Source: Medical Device Recalls)
Source: Medical Device Recalls - June 21, 2018 Category: Medical Devices Source Type: alerts