FDA-Device2026-06-24Class IIPACKAGING DEFECT
Medline convenience kits recalled for defective adhesive tubing that may crack during use
What this means
Medline convenience kits contain a recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive with defective tubing. The butyrate tubing may crack when the applicator is used, making the adhesive unusable for wound dressing or catheter applications.
- Check your Medline kit for the affected lot numbers: 25KBM985 (DYNDC3525), 26AMA168 (DT13191A), 26AMB202 (CDS982047S), or 26AMA584 (DYNJ62889C)
- Stop using any kit with a matching lot number
- Contact Medline or your supplier for a replacement kit
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
Medline convenience kits: INPATIENT CENTRAL LN DRSG KIT DYNDC3525 PICC/CVC/MIDLINE DRSG CHG KIT DT13191A PORT A CATH CDS982047S VEIN ABLATION PACK DYNJ62889C
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2419-2026More 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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