Reported Nov 15, 2023 · Ongoing
ProxiDiagnost N90, Radiography and Fluoroscopy (R/F) system
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 N90, Radiography and Fluoroscopy (R/F) system
- Lot codes and dates
- Model No. 706100 & 706110
- UDI
202 of 202 codes
(01)00884838085619(21) SN18000019(01)00884838085619(21) SN18000019(01)00884838085619(21) SN18000002(01)00884838085619(21) 721815121706(01)00884838085619(21) 10000015(01)00884838085619(21) SN18000014(01)00884838085619(21) 20000070(01)00884838085619(21) SN19000007(01)00884838085619(21) 10000035(01)00884838085619(21) 10000011(01)00884838085619(21) SN18000021(01)00884838085619(21) SN19000002(01)00884838085619(21) SN19000001(01)00884838085619(21) 10000021(01)00884838085619(21) 20000054(01)00884838085619(21) SN19000006(01)00884838085619(21) SN19000011(01)00884838085619(21) SN19000012(01)00884838085619(21) SN19000005(01)00884838085619(21) 10000051(01)00884838085619(21) 20000078(01)00884838085619(21) 10000050(01)00884838085619(21) 20000045(01)00884838085619(21) 10000008(01)00884838085619(21) SN19000018(01)00884838085619(21) 10000017(01)00884838085619(21) 10000045(01)00884838085619(21) SN19000017(01)00884838085619(21) SN19000014(01)00884838085619(21) 10000013(01)00884838085619(21) 10000010(01)00884838085619(21) 10000031(01)00884838085619(21) 10000030(01)00884838085619(21) 10000018(01)00884838085619(21) 10000024(01)00884838085619(21) 10000020(01)00884838085619(21) 10000025(01)00884838085619(21) 10000026(01)00884838085619(21) 10000028(01)00884838085619(21) SN10001008(01)00884838085619(21) 10000036(01)00884838085619(21) 10000037(01)00884838085619(21) 10000043(01)00884838085619(21) 20000026(01)00884838085619(21) SN10001004(01)00884838085619(21) 10000052(01)00884838085619(21) 20000051(01)00884838085619(21) 10001028(01)00884838085619(21) 10000040(01)00884838085619(21) 20000086(01)00884838085619(21) 20000052(01)00884838085619(21) 20000079(01)00884838085619(21) 20000068(01)00884838085619(21) 10001022(01)00884838085619(21) 20000089(01)00884838085619(21) 10001036(01)00884838085619(21) SN10001007(01)00884838085619(21) 10000023(01)00884838085619(21) SN10001002(01)00884838085619(21) 10001040
- Amount recalled
- 101 units
This recall covers 10 products
The agency filed one notice per product. You are reading one of them; the other 9 are below.
Where it was sold
- Nationwide
Why it was recalled
Potential for units suspended on the ceiling to fail and fall.
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.