---
title: "PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACH TUBE ... — FDA record Z-2591-2024 | Is It on Recall"
description: "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"
url: https://isitonrecall.com/recall/fda-device-z-2591-2024-portex-bivona-tracheostomy-silicone-tube-labeled-as-a-neonatal-trach-tube-product-code-list-number-i/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# PORTEX Bivona Tracheostomy Silicone Tube, labeled as: a) NEONATAL TRACH TUBE , Product Code/List Number/Item Code 60N... — FDA record Z-2591-2024

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date May 29, 2024. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **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.
- **Classification**: Class I
- **Recalling firm**: Smiths Medical ASD Inc.
- **Quantity**: Not supplied
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2591-2024

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2591-2024%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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, 4156652, 4176206, 4209580, 4221355, 4233978, 4238778, 4286814, 4345040, 4362872 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution.

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Sep 4, 2024
- **Recall initiation date**: May 29, 2024
- **Center classification date**: Aug 23, 2024

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2591-2024%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Smiths Medical ASD Inc. records](https://isitonrecall.com/brand/smiths-medical-asd-inc/)