FDA Device recall Z-2588-2024

PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS TRACHEOSTOMY TUBE 7.0MM TIGHT TO SHAFT CUFF, Product Code/List Number/Item Cod…

FDA Device
Class I
ongoing
Published 2024-09-04

On 2024-09-04 the FDA classified a Class I recall of PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS TRACHEOSTOMY TUBE 7.0MM TIGHT TO SHAFT CUFF, Product Code/List Number/Item Cod… by Smiths Medical Asd, citing smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defe….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2588-2024
Classification	Class I
Status	ongoing
Initiated	2024-05-29
Published	2024-09-04
Last updated	2026-09-13 11:57 UTC
Company	Smiths Medical Asd
Distribution	n/a

Product

PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS TRACHEOSTOMY TUBE 7.0MM TIGHT TO SHAFT CUFF, Product Code/List Number/Item Code 670170; b) TTS TRACHEOSTOMY TUBE 8.0MM TIGHT TO SHAFT CUFF 1/EA, Product Code/List Number/Item Code 670180

Reason

Smiths Medical has identified that the securement flange of specific lots of the Bivona Neonatal/Pediatric and Adult Tracheostomy products may tear because of a manufacturing defect.

Identifiers

code_info	a) UDI/DI 15021312006056. Product Code/List Number/Item Code 670170, Lot Numbers: 3774400, 3774401, 3774402, 3774406,… a) UDI/DI 15021312006056. Product Code/List Number/Item Code 670170, Lot Numbers: 3774400, 3774401, 3774402, 3774406, 3774411, 3774412, 3774413, 3778527, 3778528, 3778529, 3778530, 3778531, 3778532, 3778533, 3778534, 3778535, 3782488, 3782489, 3782490, 3782491, 3782492, 3790081, 3790082, 3790083, 3790084, 3790085, 3790086, 3790087, 3790088, 3790089, 3790090, 3790091, 3790092, 3790093, 3790094, 3790095, 3790096, 3790097, 3790098, 3790099, 3790100, 3797100, 3797101, 3797102, 3797103, 3797104, 3797105, 3797106, 3797107, 3797108, 3797109, 3797112, 3797113, 3797114, 3797115, 3797116, 3800538, 3800539, 3800540, 3800541, 3800542, 3800543, 3800544, 3800545, 3800546, 3800547, 3800548, 3800549, 3800550, 3800551, 3800552, 3800553, 3801603, 3801604, 3801605, 3801606, 3801607, 3801608, 3801609, 3801610, 3801611, 3801612, 3801613, 3801614, 3801615, 3801616, 3801617, 3801618, 3801619, 3801620, 3801621, 3801622, 3801623, 3801624, 3801625, 3801626, 3801627, 3801628, 3801629, 3801630, 3801631, 3801632,

code_info

a) UDI/DI 15021312006056. Product Code/List Number/Item Code 670170, Lot Numbers: 3774400, 3774401, 3774402, 3774406,…

a) UDI/DI 15021312006056. Product Code/List Number/Item Code 670170, Lot Numbers: 3774400, 3774401, 3774402, 3774406, 3774411, 3774412, 3774413, 3778527, 3778528, 3778529, 3778530, 3778531, 3778532, 3778533, 3778534, 3778535, 3782488, 3782489, 3782490, 3782491, 3782492, 3790081, 3790082, 3790083, 3790084, 3790085, 3790086, 3790087, 3790088, 3790089, 3790090, 3790091, 3790092, 3790093, 3790094, 3790095, 3790096, 3790097, 3790098, 3790099, 3790100, 3797100, 3797101, 3797102, 3797103, 3797104, 3797105, 3797106, 3797107, 3797108, 3797109, 3797112, 3797113, 3797114, 3797115, 3797116, 3800538, 3800539, 3800540, 3800541, 3800542, 3800543, 3800544, 3800545, 3800546, 3800547, 3800548, 3800549, 3800550, 3800551, 3800552, 3800553, 3801603, 3801604, 3801605, 3801606, 3801607, 3801608, 3801609, 3801610, 3801611, 3801612, 3801613, 3801614, 3801615, 3801616, 3801617, 3801618, 3801619, 3801620, 3801621, 3801622, 3801623, 3801624, 3801625, 3801626, 3801627, 3801628, 3801629, 3801630, 3801631, 3801632,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2588-2024%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.