The Recall Desk
HighFDA (Devices)·Z-1564-2018·Announced 2018-05-16

Vyaire Medical Recalls AirLife Infant Resuscitation Devices Due to Mask Sticking

Vyaire Medical is recalling 2,262 AirLife Infant Resuscitation Devices because the mask may stick to the elbow, making it difficult to disconnect.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a medical device with a functional defect that could impede emergency ventilation, representing a risk-of-harm product where injury has not yet been reported.

Plain-English summary

Vyaire Medical is recalling 2,262 units of AirLife Resuscitation, Infant, with mask, 28inch large bore tubing, and pressure-relief valve. The recall involves specific lots identified by part number 2K8019. These devices are manual resuscitation tools used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.

The recall was initiated because the mask component on various lots has been identified as having the potential to exhibit a sticking condition. This issue may result in a difficult or unable to disconnect condition of the mask from the elbow of the resuscitator.

The affected products were distributed worldwide, including in the United States (nationwide), Canada, Puerto Rico, the United Arab Emirates, the Philippines, and Europe. Consumers and healthcare providers should stop using the affected devices and contact Vyaire Medical for instructions on how to proceed.

The recalled product

Product
AirLife Resuscitation, Infant, with mask, 28inch large bore tubing, pressure-relief valve 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 adequ
Manufacturer
Vyaire Medical
Affected units
2,262

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (6)

  • Part Number: 2K8019. Lots: 0001006159
  • 0001010401
  • 0001034518
  • 0001034519
  • 0001040641
  • 0001040642

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 35 recalled by Vyaire Medical under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 35 products in this recall →