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

Recall Z-1802-2013 — BD BBL BBE // CDC Anaerobe Laked Sheep Blood Agar with KV, packaged in cartons of 100 plates, Catalog # 297260, and labeled in part Becton, Dickinson and Company 7 Loveton Circle Sparks, MD 21152 USA 800-638-8663 www.bd.com/ds Bacteroides Bile Esculin Agar (BBE) is recommended as a primary

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

AI-assisted, human-edited — this page is drafted with AI from public-source data, then reviewed before publication. How we use AI →

Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1802-2013
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

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.

Related