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

Recall Z-1949-2024 — HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006412

U.S. FDA — Device Enforcement · United States · 2024-05-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1949-2024
Date of alert
2024-05-03
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)
00884838099470
Reported risk: Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
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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