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

Recall Z-0714-2022 — KWIK-STIK, Quality control kit for culture media, sold as: KWIK-STIK (single-pack) Enterococcus faecalis derived from ATCC 51299

U.S. FDA — Device Enforcement · United States · 2014-10-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0714-2022
Date of alert
2014-10-06
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Microbiologics Inc
Product category
device
Product type
Devices
Reported risk: This strain should be resistant to high levels of Gentamicin and be resistant to Gentamicin Synergy. A specific lot was found susceptible to Gentamicin Synergy during in-house testing.
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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