FDA Device recall Z-2606-2024

PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N025

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 NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N025 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-2606-2024
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 NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N025; b) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N030; c) TTS NEONATAL TRACH TUBE , Product Code/List Number/Item Code 67N035

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 15021312006209, Product Code/List Number/Item Code 67N025, Lot Numbers: 3894899, 3949047, 4011355, 4139007,… a) UDI/DI 15021312006209, Product Code/List Number/Item Code 67N025, Lot Numbers: 3894899, 3949047, 4011355, 4139007, 4153599, 4185400, 4327887, 4331545, 4334876, 4352755, 4353076, 4372094, 4388097, 4400622; b) UDI/DI 15021312006216, Product Code/List Number/Item Code 67N030, Lot Numbers: 3853378, 3868286, 3887733, 3918002, 3939660, 4029491, 4043944, 4051629, 4060201, 4091408, 4113106, 4116109, 4128032, 4148026, 4159991, 4171571, 4185401, 4221331, 4327886, 4331548, 4334878, 4348407, 4374401, 4380992, 4380993, 4389867, 4399126; c) UDI/DI 15021312006223, Product Code/List Number/Item Code 67N035, Lot Numbers: 3868245, 3884266, 3904655, 3923736, 3952406, 3955773, 3961254, 3965335, 4016045, 4016046, 4156603, 4180470, 4216298, 4237347, 4328208, 4334879, 4344968, 4351233, 4362869, 4383593, 4395736

code_info

a) UDI/DI 15021312006209, Product Code/List Number/Item Code 67N025, Lot Numbers: 3894899, 3949047, 4011355, 4139007,…

a) UDI/DI 15021312006209, Product Code/List Number/Item Code 67N025, Lot Numbers: 3894899, 3949047, 4011355, 4139007, 4153599, 4185400, 4327887, 4331545, 4334876, 4352755, 4353076, 4372094, 4388097, 4400622; b) UDI/DI 15021312006216, Product Code/List Number/Item Code 67N030, Lot Numbers: 3853378, 3868286, 3887733, 3918002, 3939660, 4029491, 4043944, 4051629, 4060201, 4091408, 4113106, 4116109, 4128032, 4148026, 4159991, 4171571, 4185401, 4221331, 4327886, 4331548, 4334878, 4348407, 4374401, 4380992, 4380993, 4389867, 4399126; c) UDI/DI 15021312006223, Product Code/List Number/Item Code 67N035, Lot Numbers: 3868245, 3884266, 3904655, 3923736, 3952406, 3955773, 3961254, 3965335, 4016045, 4016046, 4156603, 4180470, 4216298, 4237347, 4328208, 4334879, 4344968, 4351233, 4362869, 4383593, 4395736

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-2606-2024%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.