FDAClass IINovember 22, 2023

Central Line Blood Culture DRA recall

CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562

Why was Central Line Blood Culture DRA 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 40193489402446 (case), 10193489402445 (unit): Lot Numbers: 23DMF156, 23CMH030, 23CMD955

Product
CENTRAL LINE BLOOD CULTURE DRA, REF DYNDH1562
Recalling firm
MEDLINE INDUSTRIES, LP - Northfield
Quantity
1600 kits
Distribution
US Nationwide distribution in the state of California.
Recall date
November 22, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls