MEDLINE INDUSTRIES, LP - Northfield 2025-09-03 Health critical FDA
Health · FDA · Recall #FDA-Z-2460-2025
Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic… Recall
Issued September 3, 2025 · MEDLINE INDUSTRIES, LP - Northfield
In September 2025, MEDLINE INDUSTRIES, LP - Northfield recalled the Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic…, a critical 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
Specific lots of reprocessed electrophysiology catheters may contain small residual particulates.
What you should do
- 1 Stop using Medline ReNewal Reprocessed St. Jude Medical Response and Supreme Diagnostic… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact MEDLINE INDUSTRIES, LP - Northfield 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
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Health
- Recall date
- September 3, 2025
- Units affected
- Not reported
- Sold at
- US Nationwide.
- Recall number
- FDA-Z-2460-2025
- Made in
- United States
- Issuing agency
- FDA
In context
- MEDLINE INDUSTRIES, LP - Northfield has 108 recalls in our database, including 12 rated Critical.
- We're tracking 3,576 Health recalls in our database.
- This is the 691st Health recall we've logged in 2025.