FDASeptember 23, 2023device

CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040

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

040354594069870403545940697004035459407021040354594070140403545940700704035459406994

Recall history

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

Own something like this?

AllClear screens your whole list against every CPSC, FDA, USDA and NHTSA recall — and tells you the day a new one names something you own.

Start free — 200 items, no card →