FDA Device recall Z-3089-2026
Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025
- FDA Device
- Class II
- ongoing
- Published 2026-09-09
On 2026-09-09 the FDA classified a Class II recall of Brand Name: Extension Set Product Name: DISCOFIX FOUR WAY STOPCOCK Model/Catalog Number: 456025 by B Braun Medical, citing specific lots of Discofix Stopcock Sets recalled due to an incorrect expiration date printed on the carton shipper label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3089-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2026-08-04 |
| Published | 2026-09-09 |
| Last updated | 2026-09-15 05:30 UTC |
| Company | B Braun Medical |
| Distribution | US |
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.
Identifiers
| code_info | Lot Code: Model No 456025, UDI-DI 04046964183638, Lot Numbers 0062062778 and 0062062779 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-15 05:30 UTC. Current status: ongoing.
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Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-3089-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.