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

Recall Z-2335-2016 — Zimmer¿ Air Dermatome II Handpiece w/o Hose, item number 00-8851-001-01. The Zimmer Air Dermatome II handpiece and width plates are packaged inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label is applied t

U.S. FDA — Device Enforcement · United States · 2016-07-04 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-2335-2016
Date of alert: 2016-07-04
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Zimmer Surgical Inc
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 61987607

Reported risk: The surface coating applied to the device is blistering, peeling and discoloring after usage over 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.

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