{"url_path":"/fda/device/recalls/Z-3089-2026","section_key":"summary","section_title":"DEVICE Recall: B Braun Medical Inc — Brand Name: Extension Set  Product Name: DISCOFIX FOUR WAY STOPCOCK  Model/Catalog Number: 456025","topic":"fda","document":{"doc_type":"device-recall","doc_date":"2026-08-04","source_url":"https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3089-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"B Braun Medical Inc"},"word_count":109,"has_tables":false,"body_markdown":"# FDA DEVICE Recall: Z-3089-2026\n\n**Recalling firm:** B Braun Medical Inc\n**Classification:** Class II\n**Status:** Ongoing\n**Type:** Voluntary: Firm initiated\n**Initiated:** 2026-08-04\n**Report date:** 2026-09-09\n\n## Product\nBrand Name: Extension Set  Product Name: DISCOFIX FOUR WAY STOPCOCK  Model/Catalog Number: 456025\n\n## Reason\nSpecific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.\n\n## Affected lots\nLot Code: Model No 456025, UDI-DI 04046964183638, Lot Numbers 0062062778 and 0062062779\n\n## Distribution\nWorldwide - 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."}