FDASeptember 23, 2023device

SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.

What to do

FDA enforcement status: Completed

Brands named

townsend designtownsend

UPCs

040354594070450403545940703804035459407069040354594070520403545940708304035459407076040354594071060403545940709004035459414517040354594145000403545941453104035459414524

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037 — Recall Details · AllClear