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

Recall Z-0930-2018 — Proteus 235, graphite block 8

U.S. FDA — Device Enforcement · Belgium · 2017-10-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0930-2018
Date of alert
2017-10-17
Country / jurisdiction
Belgium
Risk level
Class II
Risk type
recall
Brand
Ion Beam Applications S.A.
Product category
device
Product type
Devices
Reported risk: IBA identified incorrect screw holes depth in graphite block 8 with respect to the degrader
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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