FDA Device recall Z-1509-2021
Filtered Triple-Leg Extension Set - Intravascular administration set
- FDA Device
- Class II
- terminated
- Published 2021-05-05
On 2021-05-05 the FDA classified a Class II recall of Filtered Triple-Leg Extension Set - Intravascular administration set by B Braun Medical, citing BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1509-2021 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2021-03-15 |
| Published | 2021-05-05 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | B Braun Medical |
| Distribution | US |
Product
Filtered Triple-Leg Extension Set - Intravascular administration set. Product Catalog number: 477034 - Product Usage: The extension set is a sterile, single-use intravascular direct injection, intermittent infusion, continuous infusion or aspiration of fluids and medications.
Reason
BBMI has identified through complaints the potential for the extension set to become occluded or unable to prime.
Identifiers
| code_info | Lot #: 00SL713784, 0061741483, 0061755034, 0061755296 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1509-2021%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.