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

Recall Z-1563-2022 — DigitalDiagnost C50 1.1

U.S. FDA — Device Enforcement · United States · 2022-02-25 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1563-2022
Date of alert
2022-02-25
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Philips North America Llc
Product category
device
Product type
Devices
Reported risk: Following a system restart where the Table Height 2 (TH2) is the default setting and then switched to Wallstand VS2, operators will see an incorrect orientation of the image on the first examination due to an issue in the firmware of the Wallstand VS2 board. The system will rotate the amplimat field selection by 90 degrees. The wrong amplimat field selection may cause an incorrect dose of radiation to occur. Additionally, the anatomic position markers may become mispositioned and could potentially be associated with the opposite side of the anatomy. (Added 1/3/2023), Expansion of the root cause to include incorrect amplimat field selection by 90 degrees following the first exposure using Wallstand VS2 and a subsequent system restart. Previously, this issue only occurred following a system restart where the Table Height 2 (TH2) is the default setting.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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