Reported Jun 12, 2024 · Ongoing

HA FlexTrak-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

HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system
Product Number989710006411

Lot codes and dates: UDIN/A
Serial Numbers3 5 6 9 11 12 13 14 15 16 17 18 19 20 22 23 25 26 29 30 31 32 33 34 35 37 38 39 41 42 43 44 45 49 50 51 52 53 55 56 58 61 63 64 66 67 68 70 71 72 73 75 77 79 80 81 82 83 84 86 87 88 89 91 93 94 95 97 98
1,279 of 1,279 codes
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Amount recalled: 1348 units

The agency filed one notice per product. You are reading one of them; the other 2 are below.

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.

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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