KWIK-STIK — Class III medical device recall Z-0581-2022
Terminated recall by Microbiologics Inc, reported 2022-02-16. The incorrect lot number was printed on the foil pouch that the KWIK-STIK" is placed in. All foil pouches for
| Recall number | Z-0581-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2020-10-08 |
| Classified | 2022-02-08 |
| Reported by FDA | 2022-02-16 |
| Terminated | 2022-07-07 |
| Countries outside the US | AT, BR, CA, CH, CN, CO, DE, FI, FR, GB, GT, ID, IE, IL, IN, IT, JO, JP, KR, LT, MY, NL, NO, OM, PE, PL, RO, TH, TR, TW, VN, ZA |
| Quantity | 187 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20845357006213 |
| Lot numbers | 318-234-4 |
| Model numbers | 0318P |
Product
KWIK-STIK(TM) 2 Pack Clostridium perfringens derived from ATCC(R) 13124(TM)
Reason for recall
The incorrect lot number was printed on the foil pouch that the KWIK-STIK" is placed in. All foil pouches for lot 318-234-4 have the lot number misprinted as 218-234-4. The correct lot number was printed on the KWIK-STIK" canister label and KWIK-STIK" device label.
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-0581-2022. 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.