KWIK-STIK — Class II medical device recall Z-0876-2026
Ongoing recall by Microbiologics Inc, reported 2025-12-10. Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
| Recall number | Z-0876-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2025-11-13 |
| Classified | 2025-12-02 |
| Reported by FDA | 2025-12-10 |
| Countries outside the US | AE, CN, SG |
| Quantity | 5 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 30845357020018 |
| Lot numbers | 818-111-7 |
| Model numbers | 0818K |
Product
KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K
Reason for recall
Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.
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-0876-2026. 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.