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Recall Observatory FDA recall evidence

Device product

AirLife Resuscitation, Adult, with mask, oxygen reservoir bag, filter Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.

Z-1550-2018

April 27, 2017

Class I

Product summary

Firm
Vyaire Medical
Event
Event 78412
Status
Terminated
Classification
Class I
Quantity
1,260 units
Official record key
device-enforcement:Z-1550-2018

Official wording

Reason: The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.

Code information: Part Number: 2K8004F, Lots: 0000924948, 0000934061, 0000953218, 0000960729, 0000991584, 0001018701, 0001025673

Distribution pattern: Worldwide Distribution - US (Nationwide) and in the countries of Canada, Puerto Rico, United Arab Emirates, Philippines, and Europe.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.