Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS Recall
Issued April 2, 2025 · MEDLINE INDUSTRIES, LP - Northfield
In April 2025, MEDLINE INDUSTRIES, LP - Northfield recalled the Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS, 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
Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.
What you should do
- 1 Stop using Medline procedure kits labeled as: 1) ANGIOGRAPHY SPECIALS 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.
Recall details
- Brand
- MEDLINE INDUSTRIES, LP - Northfield
- Category
- Health
- Recall date
- April 2, 2025
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide and the country of Canada.
- Recall number
- FDA-Z-1463-2025
- 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.