The Recall Desk
HighFDA (Devices)·Z-1576-2018·Announced 2018-05-16

Vyaire Medical Recalls Pediatric AirLife Resuscitation Devices Due to Mask Sticking

Vyaire Medical is recalling 1,140 pediatric AirLife 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 used for emergency ventilation where a mechanical failure (mask sticking) could impede patient care, representing a risk-of-harm product where injury has not yet been reported.

Plain-English summary

Vyaire Medical is recalling 1,140 units of the AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, and Broselow. These manual resuscitation devices are 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 of the devices 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 are distributed worldwide, including in the United States (nationwide), Canada, Puerto Rico, the United Arab Emirates, the Philippines, and Europe. The specific part number is 2K8080BR, and the affected lots are 0000890354, 0000890352, 0000940373, 0000979974, and 0000994500.

The recalled product

Product
AirLife Resuscitation, Pediatric, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, Broselow Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breath
Manufacturer
Vyaire Medical
Affected units
1,140

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 (5)

  • Part Number: 2K8080BR. Lots: 0000890354
  • 0000890352
  • 0000940373
  • 0000979974
  • 0000994500

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 →