PlainRecalls
FDA Devices Moderate Class II Ongoing

remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use

Reported: February 26, 2025 Initiated: February 13, 2025 #Z-1201-2025

Product Description

remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use

Reason for Recall

Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.

Details

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

Frequently Asked Questions

What product was recalled?
remel BLOOD AGAR EMB AGAR BIPLATE, REF R02041, QTY 100, for invitro diagnostic use. Recalled by Remel, Inc. Units affected: 316 units.
Why was this product recalled?
Product may contain surface and subsurface contamination of Listeria monocytogenes which is typically visible immediately upon removal from the packaging, appearing on the blood side of the biplate.
Which agency issued this recall?
This recall was issued by the FDA Devices on February 26, 2025. Severity: Moderate. Recall number: Z-1201-2025.