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

Recall Z-0579-2015 — Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger Switches and Model Number ASHA5050-01: Ambient KVac Wand with Integrated Finger Switches. The Wands are indicated for the resection, ablation, and coagulation of soft tissue, and hemostasis of blood vessels in arthroscopic an

U.S. FDA — Device Enforcement · United States · 2014-10-27 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0579-2015
Date of alert: 2014-10-27
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: ArthroCare Medical Corporation
Product category: device
Product type: Devices

Reported risk: Potential breach of sterile barrier due to defective product tray.

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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