Philips North America Llc 2023-09-27 Health serious FDA
Health · FDA · Recall #FDA-Z-2608-2023
Patient Information Center iX with Software Version Number 4.x in the following: … Recall
Issued September 27, 2023 · Philips North America Llc
In September 2023, Philips North America Llc recalled the Patient Information Center iX with Software Version Number 4.x in the following: …, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Patient Information Center (PIC iX) Release 4.x Surveillance Crash Caused by Intel Graphics Driver Error-with a blank screen and subsequently require a manual reboot of the hardware to restart and continue central patient monitoring. Potential for a delay in the detection of a change or deterioration in the condition of one or more patients
What you should do
- 1 Stop using Patient Information Center iX with Software Version Number 4.x in the following: … right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips North America Llc to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Philips North America Llc
- Category
- Health
- Recall date
- September 27, 2023
- Units affected
- Not reported
- Sold at
- Nationwide Foreign: Austria Bahrain Belgium Canada Czech Republic Denmark Finland France Germany Greece India Ireland Italy Japan Jordan Ken
- Recall number
- FDA-Z-2608-2023
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips North America Llc has 34 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.