Becton Dickinson & Co. recalls BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B, 30 Single Use Test Devices- Intended for the in vitro, simultaneous…
IFU- Instructions for Use (IFU) package insert and both the IFU packaged with the test kit and the electronic version on the BD website not approved by FDA,specifically describing specimen type, could cause use of the…
Read the official notice →- Date
- 2023-06-14
- Country
- United States
- Brand
- Becton Dickinson &
- Product
- BD Veritor System for Rapid Detection of SARS-CoV-2 & Flu A+B, 30 Single Use Test Devices- Intended for the in vitro, simultaneous…
- Classification
- Class II
- Units
- Worldwide distribution - US Nationwide and the countries of CA, CL, HK, TW.
- Category
- Drugs & medical
- Source
- FDA · Device
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Becton Dickinson & recalls
- 2023-11-29
USBecton Dickinson & Company recalls BD gravity sets (Product Name, Catalog #) 32-IN GRAV SET W/0.2 MICRON FILTER BAG ACCESS PORT SS VALVE TEXIUMTM LOW ABSORPTION,…
Affected infusion sets labeled as free of DEHP actually do contain di(2-ethylhexyl) phthalate (DEHP).
FDA · DeviceBecton Dickinson & CompanyWorldwide - US Nationwide distribution including in the states of AK, AL, AR,…Official notice →- 2023-10-18
- US
Becton Dickinson & Co. recalls BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
Certain vials of the BD BACTEC" Plus Aerobic/F Culture Vials have a labeling issue where duplicate barcode sequence numbers have been identified on more than one vial.
- 2023-07-12
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Becton Dickinson & Co. recalls BD Synapsys Informatics Solution, Catalog Number 444150
There is a risk of mis-association of patient demographic data for users who choose to report results manually when their Service Control Unit (SCU) is operating near capacity and are using save actions (Skip, Final…
FDA · DeviceBecton Dickinson & Co.US States: CA, CO, IA, IL, MI, MN, MO, NY, OH, OK, SC, TN, TX, UT, WI.…Official notice → - 2023-04-26
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Becton Dickinson & Co. recalls BD Kiestra InoqulA+ with BD Kiestra" InoqulA+" and BeA Software version 5.1 and 5.1.1 as part of the Icefall A platform. An in vitro…
Upon installation of BD Kiestra" InoqulA+" and BeA version 5.1 and 5.1.1 as part of the Icefall A platform, plate information was not visible in Synapsys" after processing has occurred. This could possibly lead to a…
FDA · DeviceBecton Dickinson & Co.Worldwide - US Nationwide distribution in the states of IL, NY and the…Official notice → - 2023-03-22
- US
Becton Dickinson & Company recalls BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes…
Nonsterile syringe potentially exposing the patient to pathogenic microorganisms and a risk of local infection.
FDA · DeviceBecton Dickinson & CompanyWorldwide distribution - US Nationwide and the countries of Chile, Colombia,…Official notice → - 2022-12-21
- US
Becton Dickinson & Co. recalls BBL Chocolate II Agar- IVD for the isolation and cultivation of Neisseria species. Catalog (Ref) Number: 221267
Boxes contain a reduced concentration of Nicotinamide Adenine Dinucleotide and does not provide enough of the blood factors necessary to support Haemophilus growth. The reduction could cause a false negative result for…
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of Canada, India,…Official notice →
Other drugs & medical recalls in the United States
- 2023-06-14
- US
Bolton Medical Inc. recalls The TREO ABDOMINAL STENT-GRAFT SYSTEM (TREO) consists of four types of implants, specifically a Main Bifurcated Stent-Graft, a Leg…
Potential for the incorrect size stent-graft than the printed carton label.
FDA · DeviceBolton Medical Inc.Worldwide distribution - US Nationwide distribution in the states of FL, NY,…Official notice → - US
Avanos Medical, Inc. recalls AVNS ambIT System - PIB/PCA W 2.5in Cath, Product Code: 220509
Some of the ambIT kits were potentially distributed without an air in-line filter.
FDA · DeviceAvanos Medical, Inc.Worldwide distribution - US Nationwide distribution in the states of Texas and…Official notice → - US
Qiagen Sciences LLC recalls QIAstat-Dx Respiratory SARS-CoV-2 Panel multiplexed nucleic acid real-time PCR test, Reference Number 691223
Faulty cartridges in the lot could result in false test results.
FDA · DeviceQiagen Sciences LLCUS Nationwide distribution in the states of CA, FL, IL, MD, MS, NY, OK, PA, TN.Official notice → - US
DePuy Mitek, Inc., a Johnson & Johnson Co. recalls DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in association with…
IFU Warning: Applying bending force and/or bending force with impaction to the BIOKNOTLESS¿ Anchor Inserter may cause a fragment of the inserter tip to break off during use and be retained in the patient. broken…
FDA · DeviceDePuy Mitek, Inc., a Johnson & Johnson Co.Worldwide distribution - US Nationwide and the countries of Australia,…Official notice → - US
BioReference Health, LLC recalls The 4Kscore Test is an in vitro serum or plasma test that combines the results of four immunoassays (Roche Elecsys total PSA (prostate…
SPM software anomalies that may lead to the generation of erroneous 4Kscore Test results
FDA · DeviceBioReference Health, LLCUS Nationwide distribution in the state of New Jersey.Official notice → - US
Elekta, Inc. recalls Elekta Unity Image-Guided Radiation Therapy System containing an MR gradient coil.
There is a low possibility that an electrical connector in the MR gradient coil will overheat on Elekta Unity systems.
FDA · DeviceElekta, Inc.US Nationwide distribution in the states of FL, IA, NJ, NY, OK, PA, TN, WI,…Official notice →