Philips North America Llc 2023-11-15 Health serious FDA
Health · FDA · Recall #FDA-Z-0272-2024
DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export… Recall
Issued November 15, 2023 · Philips North America Llc
In November 2023, Philips North America Llc recalled the DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export…, 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
Potential for units suspended on the ceiling to fail and fall.
What you should do
- 1 Stop using DigitalDiagnost 4 Chest/Emergency, used to acquire, process, store, display and export… 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
- November 15, 2023
- Units affected
- Not reported
- Sold at
- Nationwide distribution.
- Recall number
- FDA-Z-0272-2024
- 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 903rd Health recall we've logged in 2023.