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Open, Classified

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

FDA Recall Z-3144-2024 · Posted 2024-09-13

Recall StatusOpen, Classified
Product CodeFPA
Date Initiated2024-08-08
Product Quantity19050 units

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.

Firm Action

An URGENT MEDICAL DEVICE RECALL NOTIFICATION letter dated 8/6/24 was sent to customers. Actions Required by B. Braun Medical Inc. (BBMI) Customer/User: 1. Review the Medical Device Recall Notification in its entirety and ensure that all users in your organization of the above-mentioned product, and other concerned persons are informed about this voluntary recall. If you are a distributor and have further distributed the product, please forward this notice to your consignees. The recall is to be extended to the consumer level. 2. Determine your current inventory of the affected items within inventory of your facility, cease use and quarantine product subject to recall. Do not destroy any affected product. 3. Utilizing the attached "Medical Device Recall Acknowledgement Form", record the total number of individual impacted units. If you have no inventory remaining, please enter zero (0) on the form. 4. Return the completed "Medical Device Recall Acknowledgement Form" to B. Braun Medical Inc. Quality Assurance department by faxing the form to (610) 849-1197 or e-mail to [email protected] within two (2) weeks of receipt, even if the total inventory in your possession is zero (0). 5. Once we receive your Medical Device Recall Acknowledgement Form, a B. Braun Customer Support representative will contact you with instructions on how to return any impacted cases, including partial cases, in your possession and provide credit and/or replacement of the product based on your individual needs. Adverse reactions or quality problems experienced with this product, or questions about this recall may be reported to BBMl's Postmarket Surveillance Department by calling 1-844-903-6417. They may also be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.

Root Cause

Process change control

Distribution Pattern

US Nationwide distribution.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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