FDA Device recall Z-2223-2025
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
- FDA Device
- Class II
- ongoing
- Published 2025-08-06
On 2025-08-06 the FDA classified a Class II recall of Blood Agar,5% Sheep Blood 100/PK, Product Number R01202 by Remel, citing the products may contain surface and subsurface contamination of Listeria monocytogenes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2223-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-07-11 |
| Published | 2025-08-06 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Remel |
| Distribution | US |
Product
Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
Reason
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Identifiers
| code_info | UDI-DI: 848838000645; Lot Numbers: 271595, 271596 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2223-2025%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.