Vitek 2 Reagent GN Test KIT Vtk2 20 Cards recall
VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341
Why was Vitek 2 Reagent GN Test KIT Vtk2 20 Cards recalled?
As the temperature and time out of range was exceeded, product performances cannot be guaranteed
What should I do if I have this product?
The recall is ongoing. Follow the firm and FDA instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
UDI/DI 03573026131913, Batch Numbers: 2412101403, 2412103403, 2412103503, 2412106403
- Product
- VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341
- Recalling firm
- Biomerieux Inc
- Quantity
- 348 units
- Distribution
- US Nationwide distribution.
- Recall date
- January 11, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)