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

Recall Z-2034-2020 — STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.

U.S. FDA — Device Enforcement · United States · 2020-01-31 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2034-2020
Date of alert
2020-01-31
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Applied Medical Resources Corp
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00607915110567
Reported risk: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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