Townsend Design FDA Recalls

3 recalls on file across devices, 0 of them Class I and 0 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 1Class IISep 23, 2023Due to potential air pockets between layers of material, the	Due to potential air pockets between layers of material, their is the potential for complete struct breakage o	Class IIDevices	Sep 23, 2023
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSXClass IISep 23, 2023Due to potential air pockets between layers of material, the	Due to potential air pockets between layers of material, their is the potential for complete struct breakage o	Class IIDevices	Sep 23, 2023
CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17CClass IISep 23, 2023Due to potential air pockets between layers of material, the	Due to potential air pockets between layers of material, their is the potential for complete struct breakage o	Class IIDevices	Sep 23, 2023