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

Recall Z-1533-2018 — BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 x 19 mm x 305 mm 23G x ¿ x 12. Catalog no 367364

U.S. FDA — Device Enforcement · United States · 2018-03-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1533-2018
Date of alert
2018-03-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Company
Product category
device
Product type
Devices
Reported risk: Products do not meet the labeled sterility claim of a Sterility Assurance Level (SAL) 10-6.
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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