FDA Device recall Z-2594-2024

PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) 3.0MM FLEXTEND NEO STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60NFPS…

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) 3.0MM FLEXTEND NEO STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60NFPS… 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-2594-2024
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) 3.0MM FLEXTEND NEO STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60NFPS30; b) 3.5MM FLEXTEND NEO STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60NFPS35; c) 4.0MM FLEXTEND NEO STRAIGHT TRACH TUBE , Product Code/List Number/Item Code 60NFPS40

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 15021312516685, Product Code/List Number/Item Code 60NFPS30, Lot Numbers: 3853441, 3868206, 3868207, 3871067… a) UDI/DI 15021312516685, Product Code/List Number/Item Code 60NFPS30, Lot Numbers: 3853441, 3868206, 3868207, 3871067, 3877651, 3887742, 3897854, 3904673, 3907995, 3926957, 3930007, 3939665, 3942472, 3946282, 3946283, 3955764, 3962605, 3982653, 3982654, 3988079, 4001201, 4008212, 4011376, 4018516, 4023788, 4029506, 4035731, 4048021, 4051634, 4053729, 4066288, 4077084, 4083942, 4092640, 4096832, 4105248, 4110445, 4122441, 4128014, 4138979, 4148025, 4159974, 4161993, 4168190, 4180503, 4185418, 4196272, 4209563, 4212773, 4218704, 4231493, 4233961, 4254232, 4276462, 4327915, 4334988, 4334989, 4345005, 4345006, 4351237, 4362840, 4369592, 4369593, 4374431, 4383622, 4389893, 4399165, 4400661; b) UDI/DI 15021312516692, Product Code/List Number/Item Code 60NFPS35, Lot Numbers: 3853442, 3868200, 3871058, 3877653, 3884262, 3887743, 3894902, 3904675, 3911432, 3918014, 3926968, 3942534, 3946286, 3952348, 3955767, 3982655, 3988080, 3988081, 3988082, 3991146, 3991147, 3991148, 3991149, 4008213,

code_info

a) UDI/DI 15021312516685, Product Code/List Number/Item Code 60NFPS30, Lot Numbers: 3853441, 3868206, 3868207, 3871067…

a) UDI/DI 15021312516685, Product Code/List Number/Item Code 60NFPS30, Lot Numbers: 3853441, 3868206, 3868207, 3871067, 3877651, 3887742, 3897854, 3904673, 3907995, 3926957, 3930007, 3939665, 3942472, 3946282, 3946283, 3955764, 3962605, 3982653, 3982654, 3988079, 4001201, 4008212, 4011376, 4018516, 4023788, 4029506, 4035731, 4048021, 4051634, 4053729, 4066288, 4077084, 4083942, 4092640, 4096832, 4105248, 4110445, 4122441, 4128014, 4138979, 4148025, 4159974, 4161993, 4168190, 4180503, 4185418, 4196272, 4209563, 4212773, 4218704, 4231493, 4233961, 4254232, 4276462, 4327915, 4334988, 4334989, 4345005, 4345006, 4351237, 4362840, 4369592, 4369593, 4374431, 4383622, 4389893, 4399165, 4400661; b) UDI/DI 15021312516692, Product Code/List Number/Item Code 60NFPS35, Lot Numbers: 3853442, 3868200, 3871058, 3877653, 3884262, 3887743, 3894902, 3904675, 3911432, 3918014, 3926968, 3942534, 3946286, 3952348, 3955767, 3982655, 3988080, 3988081, 3988082, 3991146, 3991147, 3991148, 3991149, 4008213,

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-2594-2024%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.