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

Recall Z-1422-2013 — BBL DrySlide PYR Kit, catalog number 231747 Product Usage: Presumptive diagnostic aid for group A streptococci and group D enterococci bacteria.

U.S. FDA — Device Enforcement · United States · 2013-04-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1422-2013
Date of alert
2013-04-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Co.
Product category
device
Product type
Devices
Reported risk: In-vitro diagnostic agents were placed into incorrect packaging for distribution to microbiological laboratories.
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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