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

Recall Z-0582-2022 — KWIK-STIK(TM), Streptococcus pneumoniae derived from ATCC(R) 49619(TM), packaged as follows: a. KWIK-STIK(TM) 2 Pack; b. KWIK-STIK(TM) 6 Pack. Each KWIK-STIK unit contains a lyophilized microorganism pellet, an ampoule of hydrating fluid, and an inoculating swab. Each device is sealed

U.S. FDA — Device Enforcement · United States · 2020-10-01 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0582-2022
Date of alert: 2020-10-01
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Microbiologics Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 20845357022947

Reported risk: Potential contamination with S. epidermidis E. coli and S. warneri.

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.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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