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

Recall Z-1736-2017 — CUSTOM CADAVER KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.

U.S. FDA — Device Enforcement · United States · 2017-03-09 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1736-2017
Date of alert: 2017-03-09
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Centurion Medical Products Corporation
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 2016102103

Reported risk: Centurion Medical Products is recalling Convenience Kits that contain Covidien Curity Oval Eye Pads due to supplier's recall because of potential breach in sterile packaging.

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.

Recall Z-1736-2017 — CUSTOM CADAVER KIT The Covidien Curity Oval Eye Pads are individually packaged and sterilized by the manufacturer; they are then placed into non-sterile Centurion Convenience Kits along with other components.

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