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

Recall Z-1746-2017 — BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tubes, 4.5 mL, 13 x 75 mm, Mfd: Becton Dickinson and Company Product Usage: The BD Vacutainer Safety Coagulation tube is an evacuated blood collection Tube that provides means of collecting, transporting and processing blood in a clos

U.S. FDA — Device Enforcement · United States · 2017-03-16 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1746-2017
Date of alert
2017-03-16
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Becton Dickinson & Company
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
30382903677161
Reported risk: BD is initiating this product correction of multiple lots of BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (13x75 mm x 4.5 mL). A limited number of tubes in these lots may exhibit stopper pullout from the tube as the user removes the needle from the stopper following specimen collection.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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