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…
Read the official notice →- Date
- 2023-04-26
- Country
- United States
- Brand
- Becton Dickinson &
- Product
- 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…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution in the states of IL, NY and the…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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
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- Check the product name, strength and lot number against the official notice.
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- 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
- 2023-10-18
USBecton 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
- US
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 → - 2023-06-14
- US
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…
FDA · DeviceBecton Dickinson & Co.Worldwide distribution - US Nationwide and the countries of CA, CL, HK, TW.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 → - 2022-11-23
- US
Becton Dickinson & Co. recalls BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for the rapid identification and susceptibility of most aerobic and facultative…
Misformulated minocycline-can cause erroneously increased Minimal Inhibitory Concentration (MIC) values when performing antibiotic susceptibility testing (AST) against minocycline and result in the reporting of false…
Other drugs & medical recalls in the United States
- 2023-04-26
- US
Beckman Coulter, Inc. recalls Beckman Coulter Access Free T3, Triiodothyronine, Free, Catalog #A13422, each box contains 2 reagent packs.
The reagent lot produces elevated results (approximately >30%) in some (15-20%)patient samples that do not correlate with the results of other thyroid markers nor Free T3 results generated on other platforms. This…
FDA · DeviceBeckman Coulter, Inc.Worldwide distribution - US Nationwide, including Puerto Rico and the…Official notice → - US
Olympus Corporation of the Americas recalls Single Use Rotatable Clip Fixing Device Model HX 201LR 135 - Rotatable, 165cm long, 2.8 scope channel, standard clip Model…
There have been complaints that the clip did not come out of the tube sheath during the procedure.
- US
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls SmartPerfusion, release R1.0, R1.1, R1.1.1, R1.1.5, R1.1.5.1 and R1.1.6
There are technical issues related to signal generation and processing, which can lead to inaccurate presentations.
FDA · DevicePHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Worldwide - US Nationwide distribution.Official notice → - US
NeuroLogica Corporation recalls Samsung GM85 Digital X-ray Imaging System-A Digital Diagnostic Mobile X-ray System
Issue related to the operation of the arm latch within the column that supports the arm, potential bodily harm due to a fall of the arm
- US
Medtronic Sofamor Danek USA Inc recalls INFINITY Occipitocervical Upper Thoracic System, MULTI AXIAL SCREW, Size: 4.0mm x 24mm, REF 3604024; for immobilization and…
Incorrect type of titanium was used which reduces the gripping strength of the screw head of 5 batches of Infinity Multi-Axial Screws
FDA · DeviceMedtronic Sofamor Danek USA IncWorldwide distribution - US Nationwide and the country of Canada.Official notice → - US
Medtronic Neuromodulation recalls Medtronic SenSight Extension Tunneler Kit, REF B31030; The Extension Tunneler Kit is used to assist in the tunneling and passage of…
Medtronic has received reports of SenSight Extension Tunneler kits that contain dual carriers with have been machined on only one side. As a result, the dual carrier cannot be used to pass two extensions simultaneously.
FDA · DeviceMedtronic NeuromodulationWorldwide distribution - US Nationwide and the countries of Austria, Belgium,…Official notice →