MEDLINE INDUSTRIES, LP - Northfield 2024-10-23 Health serious FDA
Health · FDA · Recall #FDA-Z-0123-2025
MEDLINE KIT CV I II, REF DYNJ906071B Recall
Issued October 23, 2024 · MEDLINE INDUSTRIES, LP - Northfield
In October 2024, MEDLINE INDUSTRIES, LP - Northfield recalled the MEDLINE KIT CV I II, REF DYNJ906071B, 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
Medline Industries, LP. has identified certain kits containing the recalled Medtronic lots of the DLP Vessel Cannulae. During manufacturing of the three listed lot numbers, product for model 30001 was incorrectly labeled as model 30000.
What you should do
- 1 Stop using MEDLINE KIT CV I II, REF DYNJ906071B 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
- October 23, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution.
- Recall number
- FDA-Z-0123-2025
- 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 737th Health recall we've logged in 2024.