Lower riskMedical device recall · FDA · Published August 4, 2026
B Braun Discofix Four Way Stopcock Recall: Incorrect Expiration Date on Carton
B Braun recalls specific lots of Discofix Four Way Stopcock sets due to incorrect expiration date on carton labels. Affected units may have expired product.
“B Braun Discofix Four Way Stopcock Recall: Incorrect Expiration Date on Carton.” GovInfoNow, updated September 16, 2026. https://govinfonow.com/recall/843290-b-braun-discofix-four-way-stopcock-recall-incorrect-expiration-date. Based on FDA recall #Z-3089-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3089-2026%22&limit=1).
B Braun Medical Inc recalled DISCOFIX FOUR WAY STOPCOCK extension sets due to incorrect expiration dates on carton labels, the FDA announced on Aug. 4, 2026. Owners should contact the company for a remedy.
How to tell if you have it
Brand: B Braun
Product Name: DISCOFIX FOUR WAY STOPCOCK
Model/Catalog Number: 456025
Lot Numbers: 0062062778 and 0062062779
The hazard
Specific lots of Discofix Stopcock Sets are recalled because an incorrect expiration date was printed on the carton shipper label.
Context
GovInfoNow's records show B Braun Medical Inc has 66 other recalls on record since Oct. 15, 2013. Other recent recalls of similar products include B. Braun Medical 100mL Sodium Chloride Injection Recall (Aug. 19, 2026) and B. Braun Medical Lactated Ringer's Injection Recall (Aug. 12, 2026). Other recent recalls of similar products include Cardinal Health ChemoPlus Gowns Recall (Nov. 12, 2025), Cook Medical Spectrum Central Venous Tray Recall (March 5, 2026) and Cook Medical Wayne Pneumothorax Tray Recall (March 5, 2026).
How to tell if you have this one
Check for the model number 456025 on the carton. Look for lot numbers 0062062778 or 0062062779. The carton may also show the UDI-DI code 04046964183638.
Brand
B Braun
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Carton Labels
Look for the model number 456025 and lot numbers 0062062778 or 0062062779 on the carton.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 18 states.
Named in the notice
Covered by “nationwide”
Not listed
FDA 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.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: California, Colorado, Florida, Georgia, Hawaii, Illinois, Indiana, Louisiana, Maryland, Massachusetts, New Jersey, New York, North Carolina, Pennsylvania, Tennessee, Texas, Virginia, Washington.
Recall timeline
FDA published this recall 36 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-3089-2026 (August 4, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-3089-2026 to see it in context.
Plain-language summary written by qwen3:4b on September 16, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.