Philips North America 2024-02-07 Health serious FDA
Health · FDA · Recall #FDA-Z-0952-2024
Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. Recall
Issued February 7, 2024 · Philips North America
In February 2024, Philips North America recalled the Intera 1.5T Achieva Nova. Model (REF) Numbers 781172., a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
The Quadrature Body Coil (QBC) seal adhesive may fail, creating sharp edges that may come in contact with patients. If the QBC seal becomes loose during the scanning process, the risk to the patient may include skin abrasions, bruises, lacerations, hair loss/entanglement, and tissue injury.
What you should do
- 1 Stop using Intera 1.5T Achieva Nova. Model (REF) Numbers 781172. right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Philips North America 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
- Category
- Health
- Recall date
- February 7, 2024
- Units affected
- Not reported
- Sold at
- Worldwide - US Nationwide distribution.
- Recall number
- FDA-Z-0952-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Philips North America has 8 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.