Home / Recalls / Remel, Inc / Z-2223-2025

Z-2223-2025 Class II Ongoing

Recalled by Remel, Inc — Lenexa, KS

Recall Details

Product Type
Devices
Report Date
August 6, 2025
Initiation Date
July 11, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1552 units

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.

Distribution Pattern

US Nationwide distribution.

Code Information

UDI-DI: 848838000645; Lot Numbers: 271595, 271596

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