FDAClass IIAugust 6, 2025

Blood Agar recall: Listeria

Blood Agar,5% Sheep Blood 100/PK, Product Number R01202

Why was Blood Agar recalled?

The products may contain surface and subsurface contamination of Listeria monocytogenes.

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: 848838000645; Lot Numbers: 271595, 271596

Product
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Recalling firm
Remel, Inc
Quantity
1552 units
Distribution
US Nationwide distribution.
Recall date
August 6, 2025
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls