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

Recall Z-0193-2020 — BD Vacutainer¿ Push Button Blood Collection Set with Pre-Attached Holder Catalog number 368356 - Product Usage: This product is designed to provide customers an increased level of safety during IV blood collection, convenience and to improve OSHA single-use holder compliance. Figure 1 shows a BD V

U.S. FDA — Device Enforcement · United States · 2019-07-31 · 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-0193-2020
Date of alert: 2019-07-31
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Becton Dickinson & Company
Product category: device
Product type: Devices

Reported risk: Separation of front and rear barrels upon activation of the safety feature that retracts the needle

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