Drug recall
1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
FDA recall event 97967 · Class II · Remel, Inc
Key facts
| Event ID | 97967 |
|---|---|
| Recall numbers | Z-0585-2026 |
| Recalling firm | Remel, Inc |
| Product type | Devices |
| Products | 1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Products may contain contamination, which may result in a darker or brown media color. |
| Initiation date | Nov 12, 2025 |
| Report date | Dec 3, 2025 |
| City | Lenexa |
| State | KS |
| Country | United States |
| FEI number | 1924669 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: