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

Recall Z-0785-2014 — ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Systems. Distributed by Philips Medical Systems, Cleveland, OH

U.S. FDA — Device Enforcement · United States · 2013-12-04 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0785-2014
Date of alert
2013-12-04
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips Medical Systems (Cleveland) Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
4750028851
Reported risk: The recalling firm determined that visual inspections of the fork joints behind the detector that are conducted during six month preventive maintenance (PM) may not detect small cracks or deficiencies in the fork weldment.
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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