Cardiac Catheterization Kit
Recall Summary Medline's PORT A CATH cardiac catheterization kits (model DYNJ906818A) are being recalled because they contain a defective batch of MASTISOL Liquid Adhesive from Ferndale Laboratories. The adhesive's butyrate tubing can crack when used, making the kit unusable for medical application. The recall affects products distributed nationwide across all U.S. states and territories.
- Product
- Medline convenience kits: PORT A CATH DYNJ906818A
- Reason
- Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.
- Classification
- Class II
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-04-27
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide distribution. OUS distribution pending.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/49276af0-2be2-42d3-a47a-1a8b870deca8