Blood/EMB recalled over Listeria risk
- Recall date
- July 11, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Official notice title
- Remel, Inc recalls Blood/EMB, Levine 100/PK, Product Number R02041
- Recall number
- Z-2225-2025
- FDA classification
- Class II
- Brand / firm
- Remel, Inc
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
Blood/EMB, Levine 100/PK, Product Number R02041
Get recall alerts
Free email alert whenever Remel, Inc has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Remel, Inc