Recall Z-3089-2026— B Braun Medical Inc

Name: FDA recall Z-3089-2026
Creator: U.S. Food and Drug Administration
Published: 2026-08-04

Class II · Ongoing

Class II FDA medical device recall by B Braun Medical Inc, initiated 2026-08-04. It names one FDA 510(k) clearance: K942988. 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..

Recalling firm: B Braun Medical Inc
Classification: Class II
Status: Ongoing
Initiated: 2026-08-04
Firm location: Bethlehem, PA, United States

510(k) clearances named in this recall

1 on FDA's record

K942988 — FILTERED EXTENSION SETSB. Braun of America, Inc.·cleared 1995-07-14

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025

Reason for recall

Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.

Data sourced from openFDA. This site is unofficial and independent of the FDA.