B Braun Medical Inc: Set, Administration, Intravascular

Recall Summary B. Braun Medical Inc is recalling specific lots of Discofix Four Way Stopcock Extension Sets because the expiration date printed on the carton label is incorrect. The product was distributed nationwide across the US and in Canada. This is a Class II recall, meaning the product could cause health problems but is unlikely to cause serious injury.

Recalling firm
B Braun Medical Inc
Product
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
Reason
Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.
Classification
Class II
Category
medical device recall
Country
United States
Agency
FDA-DEVICES
Recall date
2026-08-04
Status
Open, Classified
Areas affected
AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
Distribution
Worldwide - US Nationwide distribution in the states of CA, CO, FL, GA, HI, IL, IN, LA, MA, MD, NC, NJ, NY, PA, TN, TX, VA, WA the country of Canada.

Official recall notice from FDA-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/50f07ab1-5659-45b6-9990-73959951c345