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

Recall Z-1935-2012 — Vacuette Quickshield Complete Plus, 21G x 1 (0.8 x 25 mm), Greiner bio-one. The Quick shield Complete Plus is intended to be used only with Vacuette Blood collection Tubes as a system in routine venipuncture procedures. They are for single-use only and should only be used by adequately trained h

U.S. FDA — Device Enforcement · United States · 2012-04-02 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1935-2012
Date of alert: 2012-04-02
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Greiner Bio-One North America, Inc.
Product category: device
Product type: Devices

Reported risk: : The Quickshield Complete Plus may have a defect (split at the base), which can cause the green safety shield attachment of the Quickshield holder to be loose and unstable.

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.

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