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

Recall Z-1952-2018 — Gyrus ACMI Reusable Active Cord for Bovie/ValleyLab Generators, Catalog No C650-129A (00821925008700) The cord consists of a single conductor stranded wire terminated with plugs that connect to a generator on one end and a plug that connects to a Gyrus ACMI working element on the other end. They

U.S. FDA — Device Enforcement · United States · 2018-04-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1952-2018
Date of alert: 2018-04-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Gyrus Acmi, Incorporated
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 00821925008700

Reported risk: There is a potential for the cord to spark and cause a fire.

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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