Reported Sep 7, 2016 · Terminated
Allura Xper with release R8.2
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?
Allura Xper with release R8.2
11 of 11 products
| # | Product as published |
|---|---|
| 1 | Allura Xper FD10, 722026 |
| 2 | Allura Xper FD10/10, 722027 |
| 3 | Allura Xper FD20, 722028 |
| 4 | Allura Xper FD20/10 biplane, 722029 |
| 5 | Allura Xper FD10 OR Table, 722033 |
| 6 | Allura Xper FD10/10 OR Table, 722034 |
| 7 | Allura Xper FD20 OR Table, 722035 |
| 8 | Allure Xper FD20/20 , 722038 |
| 9 | Allura Xper FD20/20 biplane OR Table, 722039 |
| 10 | Allura Xper FD20/15, 722058 |
| 11 | Allura Xper FD20/15 OR Table, 722059 |
- Lot codes and dates
- Allura Xper with release R8.2,
- Amount recalled
- 1536 devices (includes both Allura and UNIQ)
This recall covers 4 products
The agency filed one notice per product. You are reading one of them; the other 3 are below.
Where it was sold
- Nationwide
- GA
Why it was recalled
Increase in the failure rate of certain low-voltage DC power supplies ( DCPS )
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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