Reported Apr 19, 2023 · Ongoing
CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031
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?
- CombiDiagnost R90 1.0 and 1.1 multi-functional general R/F system, Model Numbers 709030 and 709031
- Lot codes and dates
- GTIN
(01)00884838076747 (Model 709030)(01)00884838101456 (Model 709031
- Serial Numbers28 7175_04 7896_04
183 of 183 codes
100000001000000110000002100000031000000410000006100000071000001010000011100000121000001310000014100000151000001610000019100000201000002110000022100000231000002410000025100000261000002710000029100000301000003110000032100000341000003510000036100000371000003810000040100000411000004210000043100000441000004510000046100000471000004810000049100000501000005110000052100000531000005410000055100000561000005710000058100000601000006110000063100000641000006510000066100000671000006810000069
324 of 324 codes
SN16000001SN16000002SN16000003SN16000004SN16000006SN16000007SN16000008SN16000009SN17000001SN17000002SN17000003SN17000004SN17000006SN17000007SN17000008SN17000009SN17000010SN17000011SN17000012SN17000013SN17000014SN17000015SN17000016SN17000017SN17000018SN17000019SN17000020SN17000021SN17000022SN17000023SN17000024SN17000101SN17000102SN17000103SN17000104SN17000105SN17000106SN17000107SN17000108SN17000109SN17000110SN17000111SN17000112SN17000113SN17000114SN17000115SN17000116SN17000117SN17000118SN17000119SN17000120SN17000121SN17000122SN17000123SN17000124SN17000126SN17000127SN17000128SN17000129SN17000130
- GTIN
- Amount recalled
- 512 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.
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.
Free recall alerts
Get alerted about new Philips North America LLC recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.