FDA recall, , Moderate risk
B Braun Medical Discofix Four Way Stopcock Extension Sets
The Discofix Four WAY Stopcock has an incorrect expiration date printed on the carton shipper label.
Summary by Recall Canary from the FDA notice
What happened
B Braun Medical Inc of Bethlehem, Pennsylvania, recalled specific lots of the Extension Set Discofix Four Way Stopcock, model 456025, because an incorrect expiration date was printed on the carton shipper label. The company began the recall on August 4, 2026, and the FDA added it to the Enforcement Report on September 2, 2026, with classification on the same date. Distribution included nationwide in the United States across 18 states, from California to Washington, and in Canada.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number and lot code listed under your product.
Discofix Four Way Stopcock
- Model number
- 456025
- Lot code
- 0062062778
- 0062062779
Recall details
- Company began the recall
- Sold in
Worldwide - US Nationwide distribution in the states of California, Colorado, Florida, Georgia, Hawaii, Illinois, Indiana, Louisiana, Massachusetts, Maryland, North Carolina, New Jersey, New York, Pennsylvania, Tennessee, Texas, Virginia, Washington the country of Canada.
- Company
- B Braun Medical IncBethlehem, Pennsylvania
- Hazard
- Labeling error
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 99550
- Recall number
- Z-3089-2026
All recalls from B Braun Medical Inc
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
