Reported Jun 12, 2024 · Ongoing
HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system,…
Philips North America LLC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Philips North America Llc · 222 Jacobs St · Cambridge, MA · 02141-2289
Is this the product you have?
- HA FlexTrak II-Patient transport functionality to transport the patient from the preparation area to the MR system
- Product Number989710008732
- Lot codes and dates
- UDI(01)00884838099500(21)
- Serial Numbers
590 of 590 codes
100018100019100020100023100024100025100026100027100028100029100030100031100032100033100034100036100038100039100041100042100043100044100045100046100047100048100049100050100051100053100054100056100057100058100059100060100062100063100064100066100067100068100069100071100072100073100074100075100076100077100078100079100080100081100083100084100085100086100087100089
- Amount recalled
- 590 units
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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