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

Recall Z-0581-2022 — KWIK-STIK(TM) 2 Pack Clostridium perfringens derived from ATCC(R) 13124(TM)

U.S. FDA — Device Enforcement · United States · 2020-10-08 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0581-2022
Date of alert
2020-10-08
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
Microbiologics Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
20845357006213
Reported risk: The incorrect lot number was printed on the foil pouch that the KWIK-STIK" is placed in. All foil pouches for lot 318-234-4 have the lot number misprinted as 218-234-4. The correct lot number was printed on the KWIK-STIK" canister label and KWIK-STIK" device label.
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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