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Serious recall: Injury is possible or has been reported. Take action promptly.

Philips North America 2025-06-18 Health serious FDA
Health · FDA · Recall #FDA-Z-1931-2025

Intera 1.5T Achieva Nova-Dual Product Number: 781173; Recall

Issued June 18, 2025 · Philips North America

In June 2025, Philips North America recalled the Intera 1.5T Achieva Nova-Dual Product Number: 781173;, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

identified an issue where a component failure in the specific Gradient Coil type of affected systems can potentially act as a heat source, with a potential to produce smoke and/or fire. If smoke or a fire occurs, the risk to patients or operators may include inhalation of smoke, burns, and/or asphyxia which may lead to injury or even death. This issue could also lead to property damage.

What you should do

  1. 1 Stop using Intera 1.5T Achieva Nova-Dual Product Number: 781173; right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Philips North America to arrange your voluntary. See the official notice below for contact details.
  4. 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
June 18, 2025
Units affected
Not reported
Sold at
Worldwide - US Nationwide distribution in the states of AZ, CA, DE, MA, MI, MY, NE, NY, SD and the countries of Australia, Brazil, Ecuador,
Recall number
FDA-Z-1931-2025
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 691st Health recall we've logged in 2025.
Read the official FDA notice

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