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

Recall Z-2112-2012 — Beekley Altus Floral Skin Markers -Order Number: 754 Product Usage: designed for Digital Mammography-Disposable skin markers for marking areas of concern or pain

U.S. FDA — Device Enforcement · United States · 2012-07-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2112-2012
Date of alert
2012-07-09
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Beekley Corporation
Product category
device
Product type
Devices
Reported risk: Digital Skin Mammography Marker separating from the backing of the spot material
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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