FDA-Device2026-06-24Class IIPROCESSING DEFECT
Medline Centurion convenience kits recalled for defective adhesive tubing
What this means
Medline Industries' Centurion convenience kits—used for central line, dialysis, and port dressing changes—contain a recalled batch of Mastisol Liquid Adhesive with defective tubing. The tubing may crack when squeezed, making the adhesive unusable for patient care.
- Check your kit's lot number against the recall notice (lots: 2025102090, 2025102290, 2025102290, 2025111490, 2025110590).
- Do not use affected kits for patient dressing changes.
- Contact your Medline distributor or Medline directly for replacement kits.
The agency's original wording
Hazard
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Intended for
Adults
Illnesses reported
None reported
Sold states
US Nationwide distribution. OUS distribution pending.
Affected count
49,654 kits total
Manufactured in
3 Lakes Dr, Northfield, IL, United States
Products
Centurion convenience kits: CENTRAL LINE DRESSING SV43 FCP DYNDC2356B DIALYSIS CATHETER MAINTENANCE KIT DT17570 DIALYSIS DRESSING CHANGE KIT DT21370B DRESSING CHANGE TRAY - GOLD DT21115B PORT DRESSING CHANGE KIT DYNDC2815A
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2437-2026More Medline recalls
- FDA-Device2026-09-09Medline Convenience Kits recalled for potential sterility breach in antiseptic applicators
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for contamination risk
- FDA-Device2026-09-09Medline Convenience Kits recalled for sterility packaging breach risk
- FDA-Device2026-09-09Medline Convenience Kits with BD ChloraPrep Clear applicators recalled for defective packaging seals
- FDA-Device2026-09-09Medline Arterial Line Insertion Kit recalled for sterility packaging breach risk
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