This is part of a larger recall. The most authoritative record is FDA-Device / Z-0275-2027.

FDA-Device2026-10-22Class IIPACKAGING DEFECT

Medline surgical convenience kits recalled for difficult removal and skin adhesive residue

OTHERNationwide distributionMedical devices

What this means

Medline medical convenience kits used in fetal surgery, major surgery, and abdominal transplant procedures are difficult to remove from patients and may leave adhesive residue on skin. The affected kits include three product lines with specific lot numbers distributed worldwide.

  • Check if your facility uses Medline surgical convenience kits, especially Fetal Surgery CDS-LF, Major, or Abdominal Transplant kits
  • Review the lot numbers listed in the recall notice to identify affected products
  • Contact Medline or your supplier for replacement products or instructions
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The agency's original wording
Hazard

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

Intended for
Adults
Illnesses reported
None reported
Sold states
Worldwide distribution - US Nationwide and the countries of CA, TC, AU, AE.
Affected count
233 kits
Manufactured in
3 Lakes Dr, Northfield, Illinois, United States
Products
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.

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0274-2027

More Medline recalls

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