KWIK-STIK — Class III medical device recall Z-2576-2023
Ongoing recall by Microbiologics Inc, reported 2023-09-20, distributed nationwide. One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains, 6018P Parabacteroides distasonis.
| Recall number | Z-2576-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class III |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2023-08-14 |
| Classified | 2023-09-11 |
| Reported by FDA | 2023-09-20 |
| Distributed | Nationwide (US) |
| Quantity | 4 units |
| UPC / GTIN / UDI-DI | 70845357025622 |
| Lot numbers | 5065-26 |
| Model numbers | 5065P |
| Expiration dates | 2024-07-31 |
Product
KWIK-STIK, ANA (3 Strains) QC Set, REF 5065P; Microbiological testing
Reason for recall
One lot of KWIK STIK ANA (3 strains) QC Set is missing one of the strains, 6018P Parabacteroides distasonis.
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-2576-2023. 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.