Cardiac Catheterization Kit
Recall Summary Three cardiac catheterization kits (Minor Cath Lab Pack, Vascular Angio Pack, and Port-A-Cath) are being recalled nationwide because they contain a defective adhesive product that may cause tubing to crack during use, making the kits unusable. This is a Class II recall affecting medical facilities across all U.S. states and Washington, D.C.
- Product
- MINOR CATH LAB PACK DYNJ84775A OR VASCULAR ANGIO PACK DYNJ47269D PORT-A-CATH DYNJ63276G
- 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/52f5c658-8e9f-4772-83c3-f88237a03c8f