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

Recall Z-0275-2024 — DigitalDiagnost C90 Flex/Value/Chest/ER, used to acquire, process, store, display and export digital radiographic images.

U.S. FDA — Device Enforcement · United States · 2023-09-21 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0275-2024
Date of alert
2023-09-21
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips North America Llc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00884838090705
Reported risk: Potential for units suspended on the ceiling to fail and fall.
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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