Reported Oct 28, 2026 · Ongoing · Updated Nov 2, 2026

MEDLINE medical convenience kits labeled as: 1) FETAL SURGERY CDS-LF, Medline Kit Number/SKUCDS840214R; 2) MAJOR,…

Medline Industries, LP

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Medline Industries, LP · 3 Lakes Dr · Northfield, IL · 60093-2753

Is this the product you have?

  • MEDLINE
  • medical convenience kits labeled as
    • 1) FETAL SURGERY CDS-LF
    • Medline Kit Number/SKUCDS840214R
    • 2) MAJOR
    • Medline Kit Number/SKUDYNJ904851I
    • 3) ABDOMINAL TRANSPLANT
    • Medline Kit Number/SKUDYNJ908124B
Lot codes and dates

7 of 7 products

Products covered by this recall
Model / numberBarcodesProduct as published
DYNJP61011019845921762340198459217624Lot Number 26GBC179, Medline Product Number/ , UDI/DI 10198459217623 (each) 40198459217624 (case)
DYNJP61011019845921762340198459217624Lot Number 26HBV769, Medline Product Number/ , UDI/DI 10198459217623 (each) 40198459217624 (case)
DYNJP61011019845921762340198459217624Lot Number 26GBJ833, Medline Product Number/ , UDI/DI 10198459217623 (each) 40198459217624 (case)
DYNJP61061019845901264840198459012649Lot Number 26EBT593, Medline Product Number/ , UDI/DI 10198459012648 (each) 40198459012649 (case)
DYNJP61081019845901264840198459012649Lot Number 26DLB020, Medline Product Number/ , UDI/DI 10198459012648 (each) 40198459012649 (case)
DYNJP61081019845901264840198459012649Lot Number 26DLA431, Medline Product Number/ , UDI/DI 10198459012648 (each) 40198459012649 (case)
—Lot Number 26BLA251.
Amount recalled
233 kits

This recall covers 7 products

The agency filed one notice per product. You are reading one of them; the other 6 are below.

Where it was sold

  • Nationwide
  • CA

Why it was recalled

Reports of problems with product being difficult to remove from patient and leaving adhesive residue on patient's skin.

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 1:14 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.