Portex Endotracheal Tubes Recalled for Inadequate Ventilation Risk

What You Should Do

1. This recall affects Portex Endotracheal Tubes sold under item codes 100/105, 100/111, 100/126, 100/127, and 100/141.
2. Check the device packaging or hospital inventory records for specific item codes, lot numbers, and UDI-DI identifiers to determine if your supply is affected. See the Affected Products section below for the full list of affected codes.
3. Stop using the recalled device immediately to prevent patient harm.
4. Contact Smiths Medical ASD, Inc. or your clinical supply distributor to arrange for the return, replacement, or correction of the affected medical devices.
5. For further information or technical questions, contact Smiths Medical ASD, Inc. customer service directly.
6. Call the FDA: 1-888-463-6332 (1-888-INFO-FDA) for additional assistance or to report any adverse events related to these devices.

Your Remedy Options

Affected Products