KWIK-STIK 2 Pack — Class II medical device recall Z-0511-2022
Terminated recall by Microbiologics Inc, reported 2022-01-26, distributed in CA, IA, IL, LA, MA, MI, NY, PA…. Contamination with S. epidermidis
| Recall number | Z-0511-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2020-12-16 |
| Classified | 2022-01-19 |
| Reported by FDA | 2022-01-26 |
| Terminated | 2022-07-07 |
| Distributed | CA, IA, IL, LA, MA, MI, NY, PA, SD, TN, VA, WI, WV |
| Countries outside the US | BR, CA, CO, DO, FI, FR, GB, IN, JP, MX, MY, NL, PL, RO, RS, SA, ZA |
| Quantity | 59 kits |
| UPC / GTIN / UDI-DI | 10845357022964, 20845357022947, 30845357022951 |
| Lot numbers | 894-68-1, 894-68-2, 894-68-3, 894-68-4 |
| Model numbers | 0894K, 0894L, 0894P |
| Expiration dates | 2022-06-30 |
Product
KWIK-STIK 2 Pack, Catalog #0894P; KWIK-STIK 6 Pack, Catalog #0894K; and LYFO DISK, Catalog #0894L; Microsporum canis derived from ATCC 36299.
Reason for recall
Contamination with S. epidermidis
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-0511-2022. 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.