FDA recall record

B. Braun Medical AET36 ANESTH EXT SET - Anesthesia Extension Set - Normally Closed Dual recall — FDA Z-3144-2024

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…

Class IIclassification
Z-3144-2024official record ID
Sep 25, 2024report date

Recall record at a glance

Official recordZ-3144-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmB. Braun Medical, Inc.
Report dateSep 25, 2024
Recall initiation dateAug 8, 2024
Quantity19050 units
LocationAllentown, PA, United States

Official product description

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

Why the product was 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.

Distribution information

US Nationwide distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.