Reported Nov 20, 2024 · Ongoing
Philips Zenition 50, Model Number: 718096
Philips Medical Systems Nederland B.v.
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 MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 4-6 · Best, N/A · N/A
Is this the product you have?
- Philips Zenition 50
- Model Number718096
- Lot codes and dates
- Model Number718096
- UDI-DI(01)00884838091535(21)
- Serial Numbers
1,009 of 1,009 codes
79217621763174823613101311176410781759176017613171297757393915178771857501286296580147477168112888751309466467119213693863875251168916911692180741690169341515611269432798799858860936944602676701702704
- Amount recalled
- 986 units (156 US, 29 Canada, 801 ROW)
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
Why it was recalled
Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.
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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