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

Recall Z-0198-2018 — BD PhoenixTM AP, Catalog Number 448010 The BD Phoenix" AP instrument is designed for use with the BD Phoenix" system is intended to standardize ID broth tube inoculum, add AST indicator to the AST broth tube and transfer an aliquot of ID broth to AST broth tubes, as required for preparing samples f

U.S. FDA — Device Enforcement · United States · 2017-06-01 · Class III

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0198-2018
Date of alert: 2017-06-01
Country / jurisdiction: United States
Risk level: Class III
Risk type: recall
Brand: Becton Dickinson & Co.
Product category: device
Product type: Devices

Reported risk: Potential unexpected movement of robot arm

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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