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

Recall Z-2710-2016 — BD Vacutainer Push Button Blood Collection Set, Sterile, Rx only, 0.6 x 19 mm x 305 mm, 23G x 3/4" x 12", REF 367342.

U.S. FDA — Device Enforcement · United States · 2016-08-08 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2710-2016
Date of alert
2016-08-08
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Company
Product category
device
Product type
Devices
Reported risk: Becton Dickinson is recalling various lot numbers of BD Vacutainer Push Button Blood Collection Set because of reports that specific lots exhibit separation of fron and rear barrels upon activation of the safety feature, which 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.

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