Reported May 24, 2023 · Ongoing
Philips Incisive CT -Computed Tomography X-Ray System Model Number: 72814
Philips North America
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 · 222 Jacobs St · Cambridge, MA · 02141-2296
Is this the product you have?
- Philips Incisive CT -Computed
- Tomography X-Ray System Model Number72814
- Lot codes and dates
- UDI-DI(01)00884838105508(21) +
- Serial number US Serial Numbers
550243341113409234066340643404734042340253403134033
- OUS Serial NumbersSystem Serial Number
550263550249550239550215550211550091550188550187550186550174550172552041550164341075501403406255009955008255007155006855005934020550038550040550021550036550018550014550011550010550009550008550007550240550126550241
- Amount recalled
- 10 units US; 36 units OUS
This recall covers 5 products
The agency filed one notice per product. You are reading one of them; the other 4 are below.
Where it was sold
Why it was recalled
Multi-Function Foot Switch Unload Pedal Foot Entrapment-Pressing the Unload Pedal of the foot switch to perform the unload function may cause entrapment of the operator's foot and injury
This product could cause temporary or reversible health problems — stop using it.
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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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