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
Is this the product you have?
- HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system
- Product Number989710006412
- Lot codes and dates
- UDI(01)00884838099470(21)
- Serial Numbers
100 of 100 codes
1538153915401541154215431544154515461548155015521553155415561557155815591560156115631564156515661567156815691634163516361637163816391640164116421643164416461647164816491669167016721673167416751676167716781679168016811682101747101749101750101751101753
- Amount recalled
- 100 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.
Free recall alerts
Get alerted about new Philips North America LLC recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.