Portex 100/105/030

• FDA 510(k) K790312 decided 21 Feb 1979 Active
• FDA GUDID UDI-DI 15019315018640 listed 1 Sep 2015 Listed

• • Ongoing Z-1289-2025 FDA Class I ·initiated 13 Feb 2025

  Affected devices have a smaller diameter than expected and may potentially result in inadequate ventilation to the patient. Patient may experience hypoxia, underdose, or cardiopulmonary collapse.

• 4 recalls, same reason

  • Terminated Z-2538-2014 FDA Class I ·initiated 7 Jul 2014
  • Terminated Z-2537-2014 FDA Class I ·initiated 7 Jul 2014
  • Terminated Z-2539-2014 FDA Class I ·initiated 7 Jul 2014
  • Terminated Z-2536-2014 FDA Class I ·initiated 7 Jul 2014

  The tube fastener on the ET Tube Holder may compress the tracheal tube when used which may cause difficulty when locking the ET Tube Holder in place or difficulty when passing a suction catheter.

• • Terminated Z-1641-2014 FDA Class I ·initiated 10 Apr 2014

  One lot of 3.0mm sized Connectors, Product Reorder No. 10035-05PS, Lot No. 2553426 were placed in packages labeled as size 3.5mm.

1. 21 Feb 1979 Cleared FDA 510(k) K790312
2. 10 Apr 2014 Recall initiated FDA recalls Z-1641-2014
3. 7 Jul 2014 Recall initiated FDA recalls Z-2538-2014
4. 7 Jul 2014 Recall initiated FDA recalls Z-2537-2014
5. 7 Jul 2014 Recall initiated FDA recalls Z-2539-2014
6. 7 Jul 2014 Recall initiated FDA recalls Z-2536-2014
7. 1 Sep 2015 Listed FDA GUDID 15019315018640
8. 13 Feb 2025 Recall initiated FDA recalls Z-1289-2025

Trade name

Portex

Generic name

Basic endotracheal tube, single-use

Model / reference

100/105/030

Primary DI / UDI-DI

15019315018640

510(k) Number

K790312 ↗

FDA product code

BTR

GMDN term

Basic endotracheal tube, single-use

Device class

Class II

Regulation number

868.5730

GUDID distribution status

In Commercial Distribution

Category: Basic endotracheal tube, single-use

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• Bivona FT26JN30NGF219N

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• Bivona HT26JS80NSC205N

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• Bivona ST26JN55NSA204N

  Class II

  FDA 510(k) K923878 Active Cleared 29 Dec 1992 GUDID on market

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