PPM Clinical Craponne Chromid VRE 20 PLT US recall
PPM CLINICAL CRAPONNE CHROMID VRE 20 PLT US, CATALOG 43851
Why was PPM Clinical Craponne Chromid VRE 20 PLT US 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 03573026313128, Batch Numbers: 1009540400
- Product
- PPM CLINICAL CRAPONNE CHROMID VRE 20 PLT US, CATALOG 43851
- Recalling firm
- Biomerieux Inc
- Quantity
- 1 unit
- Distribution
- US Nationwide distribution.
- Recall date
- January 11, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)