FDA Device recall Z-2591-2024

PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACH TUBE , Product Code/List Number/Item Code 60N030

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) NEONATAL TRACH TUBE , Product Code/List Number/Item Code 60N030 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-2591-2024
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) NEONATAL TRACH TUBE , Product Code/List Number/Item Code 60N030; b) NEONATAL TRACH TUBE , Product Code/List Number/Item Code 60N035; c) NEONATAL TRACH TUBE , Product Code/List Number/Item Code 60N040;

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 15021312005691, Product Code/List Number/Item Code 60N030, Serial Numbers: 3853477, 3868292, 3877665, 388424… a) UDI/DI 15021312005691, Product Code/List Number/Item Code 60N030, Serial Numbers: 3853477, 3868292, 3877665, 3884248, 3904659, 3930047, 3949025, 3952381, 3955770, 3965339, 3965340, 4006289, 4051641, 4066298, 4080798, 4089297, 4110464, 4128036, 4138992, 4159934, 4171560, 4196292, 4204824, 4206834, 4212788, 4233976, 4254268, 4286813, 4331629, 4335053, 4348776, 4353055, 4358515, 4381032, 4388201, 4389921; b) UDI/DI 15021312005707, Product Code/List Number/Item Code 60N035, Serial Numbers: 3880712, 3904683, 3911437, 3946267, 3949046, 3952351, 4006291, 4023792, 4048023, 4056228, 4077083, 4086032, 4096829, 4107578, 4119113, 4136144, 4151019, 4161994, 4171561, 4180455, 4212789, 4237394, 4260075, 4279346, 4331630, 4335054, 4348749, 4348780, 4348781, 4388202, 4389922; c) UDI/DI 15021312005714, Product Code/List Number/Item Code 60N040, Serial Numbers: 3868302, 3884255, 3907990, 3931153, 3949023, 3952346, 3962603, 3982698, 3988169, 4015574, 4051633, 4089296, 4107569, 4128033, 4142419, 4

code_info

a) UDI/DI 15021312005691, Product Code/List Number/Item Code 60N030, Serial Numbers: 3853477, 3868292, 3877665, 388424…

a) UDI/DI 15021312005691, Product Code/List Number/Item Code 60N030, Serial Numbers: 3853477, 3868292, 3877665, 3884248, 3904659, 3930047, 3949025, 3952381, 3955770, 3965339, 3965340, 4006289, 4051641, 4066298, 4080798, 4089297, 4110464, 4128036, 4138992, 4159934, 4171560, 4196292, 4204824, 4206834, 4212788, 4233976, 4254268, 4286813, 4331629, 4335053, 4348776, 4353055, 4358515, 4381032, 4388201, 4389921; b) UDI/DI 15021312005707, Product Code/List Number/Item Code 60N035, Serial Numbers: 3880712, 3904683, 3911437, 3946267, 3949046, 3952351, 4006291, 4023792, 4048023, 4056228, 4077083, 4086032, 4096829, 4107578, 4119113, 4136144, 4151019, 4161994, 4171561, 4180455, 4212789, 4237394, 4260075, 4279346, 4331630, 4335054, 4348749, 4348780, 4348781, 4388202, 4389922; c) UDI/DI 15021312005714, Product Code/List Number/Item Code 60N040, Serial Numbers: 3868302, 3884255, 3907990, 3931153, 3949023, 3952346, 3962603, 3982698, 3988169, 4015574, 4051633, 4089296, 4107569, 4128033, 4142419, 4

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-2591-2024%22

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