FDA-Device2026-06-24Class IIPROCESSING DEFECT
Medline port-a-cath convenience kits recalled for defective adhesive tubing
Medline port-a-cath kits recalled for tubing defect
Medline convenience kits for port-a-cath procedures contain a recalled batch of MASTISOL Liquid Adhesive from Ferndale Laboratories. The tubing in these kits may crack during use, making the product unusable.
- Check if you have Medline port-a-cath convenience kit model DYNJ906818A.
- Do not use the kit if you have it; contact your healthcare provider or Medline for a replacement.
- Contact Medline Industries with your kit serial number (25LBC291) for instructions.
Hazard
Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
Who it affects
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: PORT A CATH DYNJ906818A
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2443-2026More Medline recalls
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