Class II

Medical Device Recall: AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036

B. Braun Medical, Inc. · August 8, 2024

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.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

19050 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-3144-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

B. Braun Medical, Inc. Medical Device Recall: AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036 | SafeCheck