Reported Jul 5, 2023 · Ongoing
DigitalDiagnost C90, Model No. 712034 and 712035
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?
DigitalDiagnost C90Model No. 712034 and 712035
- Lot codes and dates
1) UDI-DI (01)00884838090699Model 712034
- serial numbers
10000074100000831000016310000188100010571000107110001072100010791000108910001106100011331000113610001137100011421000114610001169100011801000118110001186100012031000121110001229100012341000127619861179198613652186002621860084218610012186123321861386218614152186141621861493218615282286001722860114228601152286044822860454SN19000006SN20861092SN20861107SN20861108SN20861115SN20861125SN20861126and SN20861128 2) UDI-DI (01)00884838090705Model 712035
- serial numbers
10000034100000981000105110001113100011302186004022860052SN20862021SN20862022and SN20862024
- Amount recalled
- 58
Where it was sold
Why it was recalled
There is a software login in issue that may prevent the user from logging in.
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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