AET36 ANESTH EXT SET — Class II medical device recall Z-3144-2024
Ongoing recall by B. Braun Medical, Inc., reported 2024-09-25, distributed nationwide. Potential for product leakage from the Spin Lock Connector on the distal end of the device due to the migratio
| Recall number | Z-3144-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | B. Braun Medical, Inc., Allentown, PA, United States |
| Recall initiated | 2024-08-08 |
| Classified | 2024-09-13 |
| Reported by FDA | 2024-09-25 |
| Distributed | Nationwide (US) |
| Quantity | 19,050 units |
| Reason classes | packaging |
| UPC / GTIN / UDI-DI | 04046964184659 |
| Lot numbers | 0061898815, 0061905158, 00VL872690, 00VL882317, 00VL882319 |
| Model numbers | 472036 |
Product
AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036
Reason for recall
Potential for product leakage from the Spin Lock Connector on the distal end of the device due to the migration of excess solvent during the assembly process.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-3144-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.