Drug recall
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog…
FDA recall event 97987 · Class II · Microbiologics Inc
Key facts
| Event ID | 97987 |
|---|---|
| Recall numbers | Z-0876-2026 |
| Recalling firm | Microbiologics Inc |
| Product type | Devices |
| Products | KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10. |
| Initiation date | Nov 13, 2025 |
| Report date | Dec 10, 2025 |
| City | Saint Cloud |
| State | MN |
| Country | United States |
| FEI number | 2150138 |
At a glance
- 1–9 Products in this recall
- 1–9 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: