Recall Z-2223-2025— Remel, Inc
Class II · Ongoing
Class II FDA medical device recall by Remel, Inc, initiated 2025-07-11. FDA's recall record names no specific 510(k) clearance for this event. Product: Blood Agar,5% Sheep Blood 100/PK, Product Number R01202. Reason: The products may contain surface and subsurface contamination of Listeria monocytogenes..
- Recalling firm
- Remel, Inc
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-07-11
- Firm location
- Lenexa, KS, United States
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.