Z-3089-2026 Class II Ongoing

Recalled by B Braun Medical Inc — Bethlehem, PA

FDA device recall Z-3089-2026 was initiated by B Braun Medical Inc on August 4, 2026 and is designated Class II. Reason for recall: Specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label. The recall status is ongoing. Affected quantity: 25850.

Recall Details

Product Type
Devices
Report Date
September 9, 2026
Initiation Date
August 4, 2026
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
25850

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.

Distribution Pattern

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.

Code Information

Lot Code: Model No 456025, UDI-DI 04046964183638, Lot Numbers 0062062778 and 0062062779