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

Recall Z-2434-2015 — BD Vacutainer SST Plus Blood Collection Tubes, 5.0 mL, 13 x 100 mm, Sterile. Provides a means of collecting, transporting, separating, and processing blood in a closed tube.

U.S. FDA — Device Enforcement · United States · 2015-06-23 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2434-2015
Date of alert: 2015-06-23
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Becton Dickinson & Company
Product category: device
Product type: Devices

Reported risk: Some of the tubes were manufactured with stoppers that did not meet current manufacturing specifications. Stoppers were manufactured with a reduced cycle cure time.

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.

Recall Z-2434-2015 — BD Vacutainer SST Plus Blood Collection Tubes, 5.0 mL, 13 x 100 mm, Sterile. Provides a means of collecting, transporting, separating, and processing blood in a closed tube.

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