Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
Z-1579-2018Class I

AirLife Resuscitation, Replacement kit for outer shell, Broselow

Jaeger Medical GmbH / initiated 2017-04-27 / Terminated / root cause: design

Vyaire Medical began a recall of AirLife Resuscitation, Replacement kit for outer shell, Broselow Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are... on . FDA classified it as Class I and gives the reason as "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...". As of , the recall status on record is Terminated, and MDM tags the root cause as design.

Recall record

Recall number
Z-1579-2018
Classification
Class I
Status
Terminated
Initiated
Posted
Terminated
Recalling firm
Jaeger Medical GmbH
Product
AirLife Resuscitation, Replacement kit for outer shell, Broselow 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.
Product code
OEV Cardiopulmonary Resuscitation Aid Kit
Reason for recall
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.
Root cause tag
design
FDA root cause
Component design/selection
Action
The firm, Vyaire Medical, sent an "URGENT RECALL NOTICE" letter on 04/27/2017 and again on 06/08/2017 for the expansion of the recall to its Customers. The letter described the product, problem and actions to be taken. The customers were instructed to inspect current inventory on-hand and immediately perform a 1OO% physical inventory of the product to identify and be removed; complete and return the Customer Response Form by Fax to: (312) 949.0972 or email to:[email protected].; destroy all affected product in accordance with your facility's destruction protocol; and for replacements, contact your distributor Armstrong Medical direct at (800)323.4220 x129. For any additional questions and support concerning this voluntary recall, please contact Customer Advocacy Analyst at (224) 706.6829 or email: [email protected].
Quantity in commerce
150 units
Distribution
Worldwide Distribution - US (Nationwide) and in the countries of Canada, Puerto Rico, United Arab Emirates, Philippines, and Europe.
Product codes and lots
Part Number: 7730POCH. Lots: 0000993427, 0001069517

Enforcement reports

One row per recalled product line
FDA enforcement reports joined to recall event Z-1579-2018
Recall numberClassStatusVoluntary or mandatedReport dateClassified
Z-1547-2018Class ITerminatedVoluntary: Firm initiated
Z-1548-2018Class ITerminatedVoluntary: Firm initiated
Z-1549-2018Class ITerminatedVoluntary: Firm initiated
Z-1550-2018Class ITerminatedVoluntary: Firm initiated
Z-1551-2018Class ITerminatedVoluntary: Firm initiated
Z-1552-2018Class ITerminatedVoluntary: Firm initiated
Z-1553-2018Class ITerminatedVoluntary: Firm initiated
Z-1554-2018Class ITerminatedVoluntary: Firm initiated
Z-1555-2018Class ITerminatedVoluntary: Firm initiated
Z-1556-2018Class ITerminatedVoluntary: Firm initiated
Z-1557-2018Class ITerminatedVoluntary: Firm initiated
Z-1558-2018Class ITerminatedVoluntary: Firm initiated
Z-1559-2018Class ITerminatedVoluntary: Firm initiated
Z-1560-2018Class ITerminatedVoluntary: Firm initiated
Z-1561-2018Class ITerminatedVoluntary: Firm initiated
Z-1562-2018Class ITerminatedVoluntary: Firm initiated
Z-1563-2018Class ITerminatedVoluntary: Firm initiated
Z-1564-2018Class ITerminatedVoluntary: Firm initiated
Z-1565-2018Class ITerminatedVoluntary: Firm initiated
Z-1566-2018Class ITerminatedVoluntary: Firm initiated
Z-1567-2018Class ITerminatedVoluntary: Firm initiated
Z-1568-2018Class ITerminatedVoluntary: Firm initiated
Z-1569-2018Class ITerminatedVoluntary: Firm initiated
Z-1570-2018Class ITerminatedVoluntary: Firm initiated
Z-1571-2018Class ITerminatedVoluntary: Firm initiated
Z-1572-2018Class ITerminatedVoluntary: Firm initiated
Z-1573-2018Class ITerminatedVoluntary: Firm initiated
Z-1574-2018Class ITerminatedVoluntary: Firm initiated
Z-1575-2018Class ITerminatedVoluntary: Firm initiated
Z-1576-2018Class ITerminatedVoluntary: Firm initiated
Z-1577-2018Class ITerminatedVoluntary: Firm initiated
Z-1578-2018Class ITerminatedVoluntary: Firm initiated
Z-1579-2018Class ITerminatedVoluntary: Firm initiated
Z-1580-2018Class ITerminatedVoluntary: Firm initiated
Z-1581-2018Class ITerminatedVoluntary: Firm initiated