Avea 16179

• FDA 510(k) K103211 decided 12 May 2011 Active
• FDA GUDID UDI-DI 10846446011913 listed 7 May 2021 Listed

• 12 recalls, same reason

  • Terminated Z-1894-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1888-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1892-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1897-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1895-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1896-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1898-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1899-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1889-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1890-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1893-2016 FDA Class I ·initiated 17 May 2016
  • Terminated Z-1891-2016 FDA Class I ·initiated 17 May 2016

  CareFusion has identified a potential risk associated with AVEA Ventilator caused by an incorrect F1 fuse on the AVEA Ventilator Transducer Communication Alarm (TCA) Board which may fail/blow, causing loss of power to the User Interface Module (UIM).

• • Terminated Z-1609-2015 FDA Class I ·initiated 3 Apr 2015

  A pressure transducer failure can develop, activating a false Extended High Ppeak or Circuit Occlusion Alarm. The Safety Valve will open to ambient air and the unit will stop ventilating, allowing spontaneous breathing patients to breathe. The malfunction may delay initiation or cease ventilation. Nonbreathing patients will need manual ventilation or to be connected to another ventilator.

• • Terminated Z-2273-2013 FDA Class I ·initiated 5 Sep 2013

  CareFusion has identified a potential risk associated with AVEA ventilators when used at higher altitudes. A proactive complaint review identified an error in the barometric pressure compensation. CareFusion is voluntarily initiating a field correction of the affected devices to correct the error.

• • Terminated Z-0510-2012 FDA Unclassified (pre-2012) ·initiated 8 Sep 2011

  The recall was initiated because Carefusion has identified a potential risk associated with certain AVEA ventilators and affected replacement parts manufactured between March 1, 2009 and June 30, 2011. Carefusion is voluntarily initiating a field correction of the affected devices to preclude the possibility of this risk.

1. 17 May 2016 Recall initiated FDA recalls Z-1897-2016
2. 17 May 2016 Recall initiated FDA recalls Z-1895-2016
3. 17 May 2016 Recall initiated FDA recalls Z-1896-2016
4. 17 May 2016 Recall initiated FDA recalls Z-1898-2016
5. 17 May 2016 Recall initiated FDA recalls Z-1899-2016
6. 17 May 2016 Recall initiated FDA recalls Z-1889-2016
7. 17 May 2016 Recall initiated FDA recalls Z-1890-2016
8. 17 May 2016 Recall initiated FDA recalls Z-1893-2016
9. 17 May 2016 Recall initiated FDA recalls Z-1891-2016
10. 7 May 2021 Listed FDA GUDID 10846446011913

7 earlier events are in the sections above.

Trade name

Avea

Generic name

Uninterruptible power supply

Model / Ref / Catalog

16179

Primary DI / UDI-DI

10846446011913

510(k) Number

K103211 ↗

FDA product code

CBK

GMDN term

Uninterruptible power supply

Device class

Class II

Regulation number

868.5895

GUDID distribution status

In Commercial Distribution

Category: Uninterruptible power supply

Other devices filed under FDA product code CBK (Ventilator, continuous, facility use).

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• HAMILTON-C3 by Hamilton Medical AG
• PNEUPAC VENTILATOR/RESUSCITATOR #3 by Pneupac, Ltd.
• LTV 1000 VENTILATOR by Pulmonetic Systems, Inc.
• RESPIRATOR, PROTABLE, VOLUME CONTROLLED by Dept. of the Navy
• FLIGHT 60 VENTILATOR, MODEL F-60 by Flight Medical, Ltd.
• VentStar Oxylog3000F, 2000p 300 MP00335 by Drägerwerk AG & Co. KGaA
• NEWPORT E500 WAVE VENTILATOR by Newport Medical Instruments
• FISHER & PAYKEL HEALTHCARE RT041L by FISHER & PAYKEL HEALTHCARE, INC.
• NEWPORT E360 VENTILATOR by Newport Medical Instruments

• Ltv 14982-001

  Class II

  FDA 510(k) K101643 Active Cleared 26 Jan 2011 GUDID on market

• Vmax 29122-507

  Class II

  FDA 510(k) K942211 Active Cleared 22 Nov 1994 GUDID on market

• 3100B Hfov 11744-Hrck

  Class III

  FDA PMA P890057 Active Approved 29 Mar 1991 GUDID on market

• Infant Flow™ 777000M

  Class II

  FDA 510(k) K031745 Active Cleared 13 Feb 2004 GUDID on market

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