MaXair True Low Air Loss Mattress Replacement System, True Air Technologies, Inc.
FDA Recall Z-1632-2014 · Posted 2014-05-19
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Recalling FirmSCM True Air Technologies LLC
Recall StatusTerminated
Product CodeFNM
Date Initiated2014-03-18
Date Terminated2018-06-11
Product Quantity83 units
Reason for Recall
The firm is recalling the products due to lack of design controls, lack of a Device Master Record, and failure to approve specific vendors.
Firm Action
SCM True Air Technologies LLC sent an Urgent Medical Device Recall letter to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. Customers were instructed to remove the affected product from use and return to True Air Technologies immediately. The units should be decontaminated and bagged with a certification of disinfection before return to True Air Technologies. True Air will provide replacement units to replace the returned units. Customers were instructed to refer to the Medical Device Recall Return Response Form attached for acknowledgement of receipt and contact information for this voluntary recall. Customers with questions should call 800-682-7163.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Nationwide Distribution including GA, KY, and MI.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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