Beckman Coulter Biomedical Division recalls AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their size,…
The firm has identified that the Transferrin reagent does not meet the Instructions for Use (IFU) reagent on-board stability claims, which may cause control failures and/or erroneous patient samples results. The…
Read the official notice →- Date
- 2023-11-22
- Country
- United States
- Brand
- Beckman Coulter Biomedical Division
- Product
- AU/DxC AU Chemistry Transferrin REF: OSR6152 Immune complexes formed in solution scatter light in proportion to their size, shape and…
- Classification
- Class II
- Units
- Worldwide - US Nationwide distribution including in the states of NY, CA, MS,…
- 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 Details may be shortened or out of date; the official notice is the authoritative source.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.
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FDA · DeviceAtrium Medical CorporationWorldwide distribution - US Nationwide and the countries of Algeria,…Official notice →- US
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Specific Regard kits contain the Gentige Chest Drain Products being recalled by Gentige. The Instructions for Use (IFU) for the chest drains do not provide sufficient precaution instruction for proper set up of…
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MEDLINE INDUSTRIES, LP - Northfield recalls ADLT BLOOD CULTURE COLLECT KIT, REF DYNDH1245
This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
FDA · DeviceMEDLINE INDUSTRIES, LP - NorthfieldUS Nationwide distribution in the state of California.Official notice → - US
Microbiologics Inc recalls KWIKSTIK, P. venetum, Catalog numbers: a) 0794P (2-pack), b) 0794K (6-pack)
A complaint investigation showed that the bulk pellets (lot 794-142) were contaminated with Aspergillus flavus.
FDA · DeviceMicrobiologics IncWorldwide distribution - US Nationwide and the countries of Italy, France,…Official notice → - US
Philips North America recalls Spectral CT on Rails, Software Version 5.1.0, Model Number 728334
When preparing for CCT Fluoroscopy mode and activating the CCT foot pedal simultaneously, the operator may experience a software crash. This would result in the system needing to be restarted.
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Physio-Control, Inc. recalls LIFEPAK 15, REF: 99577-000046, Part Number V15-2-000051
Their is a potential for battery pins to become loose within the defibrillator resulting in power issues.
FDA · DevicePhysio-Control, Inc.US Nationwide distribution in the states of AZ, CA, NC, NJ, NY.Official notice →