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Open, Classified

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

FDA Recall Z-3089-2026 · Posted 2026-09-02

Recalling FirmB Braun Medical Inc
Recall StatusOpen, Classified
Product CodeFPA
Date Initiated2026-08-04
Product Quantity25850

Reason for Recall

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

Firm Action

Firm began notifying customers via letter on August 4, 2026. Customers were informed that the shipper label incorrectly identifies the expiration date as 31JAN2031. The correct expiration date is listed on the individual product blisters as 01NOV2028. Customers were instructed to cease use and quarantine affected product. Product is not to be destroyed. Impacted product is to be returned to the firm for credit or replacement.

Root Cause

Under Investigation by firm

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.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K942988FILTERED EXTENSION SETSB. Braun of America, Inc. · 1995-07-14

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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