Reported Apr 19, 2023 · Ongoing
ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
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?
- ProxiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 706100 and 706110
- Lot codes and dates
- GTIN
(01)00884838085619 (Model 706100)(01)00884838103221 (Model 709031)
- Serial Numbers
243 of 243 codes
5972411000000010000001100000041000000510000006100000081000000910000010100000111000001210000013100000141000001510000016100000171000001810000019100000201000002110000022100000231000002410000025100000261000002710000028100000301000003110000032100000331000003410000035100000361000003710000039100000401000004110000042100000431000004410000045100000461000004710000048100000491000005010000051100000521000005310000054100000551000101310001014100010151000101710001018100010191000102010001021
- GTIN
- Amount recalled
- 243 units
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
Why it was recalled
If the system experiences an overvoltage / power surge it can cause a short circuit condition within the Main- cabinet. If this issue occurs, the user may experience an electrical fire within the cabinet, see or smell smoke emitting from the cabinet, or hear a popping sound coming from the cabinet.
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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