Townsend Design recalls

Townsend Design appears in 3 official U.S. recall notices indexed by RecallRadar, most recently on 2024-01-17.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V…
  FDA Device · Class II · 2024-01-17 · Townsend Design
• CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040
  FDA Device · Class II · 2024-01-17 · Townsend Design
• SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
  FDA Device · Class II · 2024-01-17 · Townsend Design