PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: August 6, 2025 Initiated: July 11, 2025 #Z-2223-2025

Product Description

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

Reason for Recall

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

Details

Recalling Firm
Remel, Inc
Units Affected
1552 units
Distribution
US Nationwide distribution.
Location
Lenexa, KS

Frequently Asked Questions

What product was recalled?
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202. Recalled by Remel, Inc. Units affected: 1552 units.
Why was this product recalled?
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 6, 2025. Severity: Moderate. Recall number: Z-2223-2025.