Instrumentation Laboratory - HemosIL ReadiPlasTin - Class 2 Recall
HemosIL ReadiPlasTin (20 mL), Part number 0020301400 (Source: Medical Device Recalls)
Source: Medical Device Recalls - November 24, 2021 Category: Medical Devices Source Type: alerts
QUICK NUMB (lidocaine) cream [Clinical Resolution Laboratory, Inc.]
Updated Date: Tue, 23 Nov 2021 00:00:00 EST (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - November 23, 2021 Category: Drugs & Pharmacology Source Type: alerts
COAGADEX (coagulation factor x human) kit [Bio Products Laboratory Limited]
Updated Date: Mon, 25 Oct 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - October 25, 2021 Category: Drugs & Pharmacology Source Type: alerts
Instrumentation Laboratory - HemosIL Liquid AntiXa
PN 0020302601: not FDAcleared; not sold in the US - Class 2 Recall
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACLTOP¿ Family, ACL TOP Family 50 Seriest and ACL Elite¿/Elite Pro) Part Number: 0020302601 (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 20, 2021 Category: Medical Devices Source Type: alerts
Instrumentation Laboratory - HemosIL Liquid AntiXa - Class 2 Recall
HemosIL Liquid Anti-Xa- automated chromogenic assay for in vitro diagnostic use by laboratory professionals in clinical laboratories. The assay provides quantitative results on 3.2% citrated human plasma Part Number: 0020302602 (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 20, 2021 Category: Medical Devices Source Type: alerts
Instrumentation Laboratory - HemosIL Liquid AntiXa - Class 2 Recall
HemosIL Liquid Anti-Xa- Automated chromogenic assay for the quantitative determination of unfractionated heparin (UFH) and low molecular weight heparin (LMWH) activity in human citrated plasma on IL Coagulation Systems, (ACL TOP¿ Family, ACL TOP Family 50 Seriest and ACL Elite¿/Elite Pro/8/9/10000) Part Number: 0020302600 (Source: Medical Device Recalls)
Source: Medical Device Recalls - October 20, 2021 Category: Medical Devices Source Type: alerts
Green Field Farms Dairy Issues Voluntary Recall of Whole Chocolate Milk
Green Field Farms Dairy of Fredericksburg, Ohio announces a voluntary recall of its Whole Chocolate Milk product, with a code date of 9/29/21, due to a laboratory analysis that indicated this product was not effectively pasteurized. 1,242 units of the affected product were distributed in Ohio, India (Source: FDA Food Safety)
Source: FDA Food Safety - September 17, 2021 Category: Food Science Authors: FDA Source Type: alerts
RITUAL TATTOO REVEAL FOAM (lidocaine, tetracaine, witch hazel) liquid [MK Laboratory]
Updated Date: Wed, 15 Sep 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 15, 2021 Category: Drugs & Pharmacology Source Type: alerts
RITUAL TATTOO (lidocaine, tetracaine, witch hazel) spray [MK Laboratory]
Updated Date: Wed, 15 Sep 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 15, 2021 Category: Drugs & Pharmacology Source Type: alerts
RITUAL TATTOO (lidocaine, tetracaine) lotion [MK Laboratory]
Updated Date: Wed, 15 Sep 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 15, 2021 Category: Drugs & Pharmacology Source Type: alerts
DESMAQUILLANTE OJOS WEYE (makeup remover) cream LIMPIADOR DE OJOS WEYE (eye cleansing) gel [WEYE LABORATORY GROUP S.L.]
Updated Date: Wed, 08 Sep 2021 00:00:00 EDT (Source: DailyMed Drug Label Updates)
Source: DailyMed Drug Label Updates - September 8, 2021 Category: Drugs & Pharmacology Source Type: alerts
Versea Diagnostics LLC - Healgen COVID19 IgG/IgM Rapid Test Cassette - Class 2 Recall
Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) Qualitative detection and differentiation of IgM and IgG antibodies against SARS-CoV-2 in human venous whole blood, plasma (Li+- heparin, K2-EDTA and sodium-citrate), and serum. Intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection. Emergency use of this test is limited to authorized laboratories. Authorized Laboratories: Laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. 263a, to perform moderate or high complexity te...
Source: Medical Device Recalls - September 4, 2021 Category: Medical Devices Source Type: alerts
Beckman Coulter Inc. - Normand Info Remisol Advance Data Manager - Class 2 Recall
Normand Remisol Advance Data Manager, REF: C69412, C69413, C44703, and C57017 is a software device that interfaces between laboratory information systems (LIS) and laboratory instruments. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 24, 2021 Category: Medical Devices Source Type: alerts
Stanbio Laboratory, LP - Hydroxybutyrate LiquiColor - Class 3 Recall
Beta-Hydroxybutyrate LiquiColor. in vitro diagnostic reagent. (Source: Medical Device Recalls)
Source: Medical Device Recalls - August 6, 2021 Category: Medical Devices Source Type: alerts
