# FDA recall Z-1950-2024

> **Philips North America Llc** · Class II · device recall initiated 2024-05-03.

## 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

## 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, Japan, Jordan, Lithuania, Martinique, Mexico, Morocco,  Netherlands, Norway, Oman, Peru, Poland, Russian Fed., Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, United Kingdom.

## Key facts

- **Recall number:** Z-1950-2024
- **Recalling firm:** Philips North America Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-05-03
- **Report date:** 2024-06-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Cambridge, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1950-2024

## Citation

> AI Analytics. FDA recall Z-1950-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1950-2024. Source: US FDA. Licensed CC0.

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