KWIK-STIK — Class III medical device recall Z-0641-2022
Terminated recall by Microbiologics Inc, reported 2022-02-23, distributed nationwide. Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the
| Recall number | Z-0641-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2013-03-25 |
| Classified | 2022-02-14 |
| Reported by FDA | 2022-02-23 |
| Terminated | 2022-04-22 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA, CN, FR, NL, ZA |
| Quantity | 10 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 20845357029502 |
| Lot numbers | 1023-05-7 |
| Model numbers | 01023P |
Product
KWIK-STIK(TM), Quality control kit for culture media, sold as: KWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)
Reason for recall
Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating this is a labeling error and the organism is the correct organism.
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-0641-2022. 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.