KWIK-STIK — Class III medical device recall Z-0543-2022
Terminated recall by Microbiologics Inc, reported 2022-02-09, distributed in GA, MS, MT, NC, NM, NV, TN, TX…. Potential that products packaged for lot 726-57-10 were packaged in pouches labeled as 323-108-7.
| Recall number | Z-0543-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2021-02-24 |
| Classified | 2022-01-28 |
| Reported by FDA | 2022-02-09 |
| Terminated | 2022-07-11 |
| Distributed | GA, MS, MT, NC, NM, NV, TN, TX, WA, WI |
| Countries outside the US | AE, BR, CA, CN, CO, DO, FR, IE, IN, JP, MX, OM, PH, RO, TR, ZA |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20845357017486 |
| Lot numbers | 726-57-10 |
| Model numbers | 0726P |
Product
KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.
Reason for recall
Potential that products packaged for lot 726-57-10 were packaged in pouches labeled as 323-108-7.
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-0543-2022. 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.