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

Recall Z-2338-2016 — Zimmer¿ Air Dermatome II Width Plate, 1.5 inch. Part #00-8851-215-00. Width plate is packaged inside of a padded-foam corrugate box. A product label is applied to the lid of the box. The width plates, when sold individually, are placed in a labeled poly zipper bag, which is then placed into a

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-2338-2016
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): 61999884

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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