Reported May 10, 2023 · Ongoing
Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general…
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?
- Philips ProxiDiagnost N90 1.0 (Model 706100) and ProxiDiagnost N90 1.1 (Model 706110)- A multi-functional general radiography and fluoroscopy (R/F) system
- Lot codes and dates
- UDI(01)00884838085619(21) ProxiDiagnost N90 1.0 (706100); (01)00884838103221(21) ProxiDiagnost N90 1.1 (706110)
- Serial NumbersSerial Number
234 of 234 codes
5972411000000010000001100000041000000510000006100000081000000910000010100000111000001210000013100000141000001510000016100000171000001810000019100000201000002110000022100000231000002410000025100000261000002710000028100000301000003110000032100000331000003410000035100000361000003710000039100000401000004110000042100000431000004410000045100000461000004710000048100000491000005010000051100000521000005310000054100000551000101310001014100010151000101710001018100010191000102010001021
- Amount recalled
- Total Quantity: 234 units. US 195units. R.O.W 39 units
Where it was sold
- Nationwide
- PR
Why it was recalled
Potential table stop due to a broken tabletop cable: On the ProxiDiagnost N90 table there is a cable located under the tabletop that is covered by a plastic sleeve which can crack and damage the cable. If the tabletop cable breaks, the user may not be able to initiate table tilting movements or braking
This product could cause temporary or reversible health problems — stop using it.
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