24 Blood Culture KIT recall
24 BLOOD CULTURE KIT, REF DYNDH1632
Why was 24 Blood Culture KIT recalled?
This recall is being issued due to items within the kit have expired prior to the overall kit expiration date listed on the insert.
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 40193489916141 (case), 10193489916140 (unit): Lot Numbers: 23EMF710, 23DMF154, 23DMA779
- Product
- 24 BLOOD CULTURE KIT, REF DYNDH1632
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 3160 kits
- Distribution
- US Nationwide distribution in the state of California.
- Recall date
- November 22, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)