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

Recall Z-1798-2013 — BD BBL Vancomycin Screen Agar, carton of 10 plates, catalog # 222204, labeled in part Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds Vancomycin Screen Agar is used to test entercocci for resistance to vancomycin and to predict the synergistic

U.S. FDA — Device Enforcement · United States · 2013-06-06 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1798-2013
Date of alert: 2013-06-06
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Becton Dickinson & Co.
Product category: device
Product type: Devices

Reported risk: Microbiological identification media may exhibit reduced levels of Vancomycin.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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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