Philips North America Llc 2024-05-22 Health serious FDA
Health · FDA · Recall #FDA-Z-1827-2024
Patient Information Center iX and Patient Information Center iX Expand, Software Version… Recall
Issued May 22, 2024 · Philips North America Llc
In May 2024, Philips North America Llc recalled the Patient Information Center iX and Patient Information Center iX Expand, Software Version…, 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
Event Catalog information does not save when copied and transferred from one unit to another.
What you should do
- 1 Stop using Patient Information Center iX and Patient Information Center iX Expand, Software Version… 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
- May 22, 2024
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution in the states of CA, FL, GA, IA, MA, MI, MN, MO, NJ, NM, NY, OH, PA, TN, TX, WA, WV, & DC. The countr
- Recall number
- FDA-Z-1827-2024
- 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 737th Health recall we've logged in 2024.