KWIK-STIK" plus: Clostridium perfringens — Class III medical device recall Z-1125-2022
Terminated recall by Microbiologics Inc, reported 2022-06-01, distributed nationwide. Labeling error.
| Recall number | Z-1125-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2022-05-06 |
| Classified | 2022-05-23 |
| Reported by FDA | 2022-06-01 |
| Terminated | 2024-01-16 |
| Distributed | Nationwide (US) |
| Countries outside the US | CO, FR, GB, MX, ZA |
| Quantity | 8 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20845357019374 |
| Lot numbers | 801-44-4 |
| Model numbers | 0801P |
| Expiration dates | 2023-05-31 |
Product
KWIK-STIK" plus: Clostridium perfringens
Reason for recall
Labeling error.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1125-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.