Drug recall
KWIK-STIK" plus: Clostridium perfringens
FDA recall event 90150 · Class III · Microbiologics Inc
Key facts
| Event ID | 90150 |
|---|---|
| Recall numbers | Z-1125-2022 |
| Recalling firm | Microbiologics Inc |
| Product type | Devices |
| Products | KWIK-STIK" plus: Clostridium perfringens |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Labeling error. |
| Initiation date | May 6, 2022 |
| Report date | Jun 1, 2022 |
| Termination date | Jan 16, 2024 |
| 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: