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Townsend Design Recalls
3 recalls on record · January 17, 2024 to January 17, 2024 · Medical Devices
January 17, 2024Medical DevicesFDA
Townsend Design recalls SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
Hazard: Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
January 17, 2024Medical DevicesFDA
Townsend Design recalls SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 1
Hazard: Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
January 17, 2024Medical DevicesFDA
Townsend Design recalls CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C
Hazard: Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.