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

Recall Z-2976-2018 — Art-Line Surgery Pack-LF, STERILE, 40 packs each per case.

U.S. FDA — Device Enforcement · United States · 2017-04-12 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2976-2018
Date of alert
2017-04-12
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Medline Industries, Inc.
Product category
device
Product type
Devices
Reported risk: Multiple surgical packs were assembled with a non-sterile CHG disk labeled as BIOPATCH" (kit component #52655) attached to the outside of the sterile pack. This may pose potential risk of infection. However, the kits have been in distribution since March 2016. Many of these kits have been used with no reported infections or adverse patient events. In addition, the BIOPATCH is impregnated with CHG, a well-known antiseptic agent with broad-spectrum anti-microbial and antifungal activity.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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