Medline Industries, Lp: Angiography/angioplasty Kit

Recall Summary Medline Industries is recalling CABG AUXILIARY PACK surgical kits (Product Number DYNJ44925D) distributed nationwide because the cannula components inside don't meet required dimensional standards and may leak or break during use. The kits were sent to healthcare facilities across all U.S. states and the District of Columbia. This is a Class II recall involving medical devices.

Recalling firm
Medline Industries, LP
Product
Medline surgical convenience kits labeled as: CABG AUXILIARY PACK, Medline Product Number/SKU DYNJ44925D
Reason
Medical convenience kits were distributed containing cannula components which do not conform to ISO 80369-7 dimensional requirements and may contribute to leaking or breaking during use.
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-09-02
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
US Nationwide distribution.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/822e3fef-5e21-4e36-b168-1735c308b441