Peripheral Blood Culture Draw recall
PERIPHERAL BLOOD CULTURE DRAW, REF DYNDH1561
Why was Peripheral Blood Culture Draw 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 40193489402811 (case), 10193489402810 (unit): Lot Numbers: 23EMF711, 23CMH027
- Product
- PERIPHERAL BLOOD CULTURE DRAW, REF DYNDH1561
- Recalling firm
- MEDLINE INDUSTRIES, LP - Northfield
- Quantity
- 1770 kits
- Distribution
- US Nationwide distribution in the state of California.
- Recall date
- November 22, 2023
- Classification
- Class II
- Status
- Ongoing
- Agency
- FDA (device)