Recall Z-2593-2023— Aquila Corporation

Name: FDA recall Z-2593-2023
Creator: U.S. Food and Drug Administration
Published: 2023-07-06

Class II · Ongoing

Class II FDA medical device recall by Aquila Corporation, initiated 2023-07-06. FDA's recall record names no specific 510(k) clearance for this event. Product: APK2 Pressure-Sensing Wheelchair Cushions. Reason: Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury..

Recalling firm: Aquila Corporation
Classification: Class II
Status: Ongoing
Initiated: 2023-07-06
Firm location: Holmen, WI, United States

Product description

APK2 Pressure-Sensing Wheelchair Cushions

Reason for recall

Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.

Data sourced from openFDA. This site is unofficial and independent of the FDA.