Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0543-2022 — KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.

U.S. FDA — Device Enforcement · United States · 2021-02-24 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0543-2022
Date of alert
2021-02-24
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Microbiologics Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20845357017486
Reported risk: Potential that products packaged for lot 726-57-10 were packaged in pouches labeled as 323-108-7.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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