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

Recall Z-1739-2017 — Covidien Curity Eye Pad Item Code: 03201 The sterile eye pad is a device that consists of a pad made of various materials, such as gauze and cotton, intended for use as a bandage over the eye for protection or absorption of secretions. It is supplied sterile to allow for use in the operating room

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

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1739-2017
Date of alert: 2017-03-03
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Covidien LLC
Product category: device
Product type: Devices

Reported risk: Product sterility is compromised due to breach of sterile barrier

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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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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