Reported Feb 1, 2017 · Terminated
Velara Generator with an old Firmware version used with the Philips Integris BH5000
Philips Electronics North America Corporation
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 Electronics North America Corporation · 3000 Minuteman Rd · Andover, MA · 01810-1032
Is this the product you have?
- Velara Generator with an old Firmware version used with the Philips Integris BH5000
- Lot codes and dates
- Velara Generator with 12nc number
989000070011989000070122989000070123989000070124989000070125989000070126989000070321
- Velara Generator with 12nc number
- Amount recalled
- 59 devices (this number represents all products listed in recall)
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
Why it was recalled
System may lock up.
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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