Philips North America Llc Recall: HA FlexTrak II-Patient transport functionality to transp
Philips North America Llc Recall: HA FlexTrak II-Patient transport functionality to transp is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips North America Llc; Product: HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR sys
| Recalling firm | Philips North America Llc |
|---|---|
| Product | HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710008732 |
| Reason for recall | Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain, Bangladesh, Belgium, Brazil, Canada, Chile, China, Colombia, Czech Republic, Denmark, Estonia, Fiji, Finland, France, French Guiana, Germany, Guadeloupe, Honduras, Hong Kong, India, Indonesia, Ireland, Italy, Ja |
| Recall initiated | 20240503 |
| Recall number | Z-1950-2024 |
| Category | device |
| State | MA |
| Country | United States |
$29/mo
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