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Townsend Design recalls CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C
Recalled January 17, 2024 · FDA recall Z-0670-2024 · Townsend Design
Hazard
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis. · FDA Class II
Units
248 units
Sold at
US: AL AR AZ CA CO CT DC DE FL GA IA ID IL IN KENT KS KY LA MA MD ME MI MN MO MS MT NC NE NH NJ NM NV NY OH OK OR PA QC SC SD TN TX UT VA VT WA WI WV WY, Puerto Rico, OUS: None OUS: Canada, New Zealand, Japan, Australia, Netherlands, United Kingdom
Description
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
Product
CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040
Manufacturer(s)
Townsend Design
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →