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MEDLINE INDUSTRIES, LP - Northfield 2025-04-02 Health serious FDA
Health · FDA · Recall #FDA-Z-1439-2025

Medline procedure kits labeled as: 1) AV FISTULA PACK-LF, Pack Number DYNJ0826753O; … Recall

Issued April 2, 2025 · MEDLINE INDUSTRIES, LP - Northfield

In April 2025, MEDLINE INDUSTRIES, LP - Northfield recalled the Medline procedure kits labeled as: 1) AV FISTULA PACK-LF, Pack Number DYNJ0826753O; …, 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. 1 Stop using Medline procedure kits labeled as: 1) AV FISTULA PACK-LF, Pack Number DYNJ0826753O; … right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact MEDLINE INDUSTRIES, LP - Northfield 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
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-1439-2025
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.
Read the official FDA notice

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