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

Recall Z-0804-2015 — Radiomat M+ NIF 14 x 17, Radiomat M+ NIF 35CM x 43CM, Radiomat M+ NIF 10 x 12, Radiomat M+ NIF 25,4CM x 30,5CM

U.S. FDA — Device Enforcement · United States · 2014-10-24 · Class III

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0804-2015
Date of alert
2014-10-24
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
AGFA Healthcare Corp.
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
79440009
Reported risk: Some material of the coating Type CXCPMV3 has potential artifacts showing a small bright thin line when the film is processed.
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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