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

Recall Z-2592-2016 — MAMMOGRAPHY

U.S. FDA — Device Enforcement · United States · 2015-10-05 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2592-2016
Date of alert
2015-10-05
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Avid Medical, Inc.
Product category
device
Product type
Devices
Reported risk: Avid Medical Inc. states a latex-containing Telfa" Non-adherent Dressing 4"x3" (10.2cm x 7.6 em) was included in a limited number of convenience kits (custom procedure trays) that were not labeled as containing latex.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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