FDA Device recall Z-2224-2025
Strep Selective II Agar, Product Number R01859
- FDA Device
- Class II
- ongoing
- Published 2025-08-06
On 2025-08-06 the FDA classified a Class II recall of Strep Selective II Agar, Product Number R01859 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-2224-2025 |
| 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
Strep Selective II Agar, Product Number R01859
Reason
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Identifiers
| code_info | UDI-DI: 848838003158; Lot Numbers: 271613 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Other recalls by Remel
- GC Agar Base (150mm) 10/PK R04030
FDA Device · Class II · 2026-07-08 · Remel - Yeastone Broth, 11ML, 10/BOX YY3462
FDA Device · Class II · 2026-04-22 · Remel - Campy CVA Medium 100/PK, R01272
FDA Device · Class II · 2026-03-04 · Remel - 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
FDA Device · Class II · 2025-12-03 · Remel - Blood Agar,5% Sheep Blood 100/PK, Product Number R01202
FDA Device · Class II · 2025-08-06 · Remel
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2224-2025%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.