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

Recall Z-1892-2018 — Southmedic Sterile Disposable Scalpel Rx only Scalpels are intended to be used in various medical procedures for preparation, scraping and/or cutting of tissue.

U.S. FDA — Device Enforcement · Canada · 2017-11-06 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1892-2018
Date of alert
2017-11-06
Country / jurisdiction
Canada
Risk level
Class II
Risk type
recall
Brand
Southmedic, Inc.
Product category
device
Product type
Devices
Reported risk: Scalpels lot contains non-sterile products labeled as sterile.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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