Drug recall
AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock…
FDA recall event 95153 · Class II · B. Braun Medical, Inc.
Key facts
| Event ID | 95153 |
|---|---|
| Recall numbers | Z-3144-2024 |
| Recalling firm | B. Braun Medical, Inc. |
| Product type | Devices |
| Products | AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| 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. |
| Initiation date | Aug 8, 2024 |
| Report date | Sep 25, 2024 |
| City | Allentown |
| State | PA |
| Country | United States |
| FEI number | 2523676 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: