FDA-Device2026-10-22Class IIPROCESSING DEFECT

Medline tubal ligation surgical kit recalled for difficult removal and skin adhesive residue

OTHERNationwide distributionMedical devices

What this means

Medline's tubal ligation surgical convenience kit (SKU DYNJ906291G) is difficult to remove from patients and can leave adhesive residue on skin. A small number of kits (3 total) with lot number 26GBQ124 have been distributed worldwide.

  • If you have this kit in your facility, check for lot number 26GBQ124 on the packaging.
  • Contact Medline for instructions on returning or disposing of affected kits.
  • Report any patient skin irritation or adhesive residue issues to Medline and the FDA.
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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
3 kits
Manufactured in
3 Lakes Dr, Northfield, Illinois, United States
Products
MEDLINE medical convenience kits labeled as: TUBAL LIGATION RFD, Medline Product Number/SKU DYNJ906291G

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0279-2027

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