FDA recall Z-2224-2025
Remel, Inc · Class II · device
Product
Strep Selective II Agar, Product Number R01859
Reason for recall
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Distribution
US Nationwide distribution.
Key facts
- Status
- Ongoing
- Initiation date
- 2025-07-11
- Report date
- 2025-08-06
- Voluntary/Mandated
- Voluntary: Firm initiated
- Location
- Lenexa, KS, United States
Primary source
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2224-2025