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

Recall Z-0813-2018 — Surgical punch; sealed pouches packed in punch shelf box Intended for use by trained surgeons to create circular cuts in soft tissue or openings in soft vessel walls during surgical procedures.

U.S. FDA — Device Enforcement · United States · 2017-10-23 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0813-2018
Date of alert
2017-10-23
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Alto Development Corp
Product category
device
Product type
Devices
Reported risk: Surgical punches are being recalled due to potential packaging damage which may have occurred during transportation resulting in loss of sterility.
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.