Carestream Health, Inc. 2023-12-13 Health serious FDA
Health · FDA · Recall #FDA-Z-0437-2024
DRX Revolution Mobile X-Ray System Recall
Issued December 13, 2023 · Carestream Health, Inc.
In December 2023, Carestream Health, Inc. recalled the DRX Revolution Mobile X-Ray System, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Unexpected failure of electrical components within the CPI generator.
What you should do
- 1 Stop using DRX Revolution Mobile X-Ray System right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Carestream Health, Inc. 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
- Carestream Health, Inc.
- Category
- Health
- Recall date
- December 13, 2023
- Units affected
- Not reported
- Sold at
- Worldwide Distribution: US (Nationwide Distribution); and OUS (Foreign): Algeria, Argentina, Australia, Austria, Bahrain, Belarus, Belgium,
- Recall number
- FDA-Z-0437-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Carestream Health, Inc. has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 903rd Health recall we've logged in 2023.