Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold Recalled by B. Braun Medical, Inc. Due to Potential for product leakage from the Spin Lock...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact B. Braun Medical, Inc. directly.
Affected Products
AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual Manifold, Four-way Stopcock, Model/Catalog Number: 472036
Quantity: 19050 units
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About B. Braun Medical, Inc.
B. Braun Medical, Inc. has 216 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report