FDA Device recall Z-1950-2024
HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100…
- FDA Device
- Class II
- ongoing
- Published 2024-06-12
On 2024-06-12 the FDA classified a Class II recall of HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100… by Philips North America, citing oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1950-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-03 |
| Published | 2024-06-12 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710008732
Reason
Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
Identifiers
| code_info | UDI: (01)00884838099500(21) Serial Numbers: 100018 100019 100020 100023 100024 100025 100026 100027 100028 100029 10003…UDI: (01)00884838099500(21) Serial Numbers: 100018 100019 100020 100023 100024 100025 100026 100027 100028 100029 100030 100031 100032 100033 100034 100036 100038 100039 100041 100042 100043 100044 100045 100046 100047 100048 100049 100050 100051 100053 100054 100056 100057 100058 100059 100060 100062 100063 100064 100066 100067 100068 100069 100071 100072 100073 100074 100075 100076 100077 100078 100079 100080 100081 100083 100084 100085 100086 100087 100089 100090 100091 100092 100093 100094 100095 100096 100097 100098 100099 100100 100102 100103 100104 100105 100106 100107 100108 100109 100110 100111 100112 100113 100114 100115 100116 100117 100118 100119 100120 100121 100122 100123 100124 100125 100126 100127 100129 100130 100131 100133 100134 100135 100136 100137 100138 100140 100141 100143 100144 100145 100146 100148 100149 100150 100152 100153 100154 100155 100156 100157 100158 100159 100161 100164 100165 100166 100167 100170 100171 100172 100174 100175 100176 100177 100178 1001 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1950-2024%22
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