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

Recall Z-1189-2017 — BD Vacutainer Buffered Sodium Citrate: (9NC) Blood Collection Tube (4.5 ml x 13 x 75 mm) Catalog Number: 369714 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 closed tube.

U.S. FDA — Device Enforcement · United States · 2017-01-16 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1189-2017
Date of alert: 2017-01-16
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Becton Dickinson & Company
Product category: device
Product type: Devices

Reported risk: A portion of this lot of blood collection tubes was manufactured with approximately twice the expected amount of buffered sodium citrate additive, an anticoagulant.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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.

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