FDA Device recall Z-0671-2024
SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V…
- FDA Device
- Class II
- completed
- Published 2024-01-17
On 2024-01-17 the FDA classified a Class II recall of SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V… by Townsend Design, citing due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0671-2024 |
| Classification | Class II |
| Status | completed |
| Initiated | 2023-09-23 |
| Published | 2024-01-17 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Townsend Design |
| Distribution | AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
Product
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
Reason
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
Identifiers
| code_info | REF: 17V1030/UDI: (01)04035459407045/ Order #s 877130 871608 869477 873755 873408 873462 872532 871154 880168 880929 86…REF: 17V1030/UDI: (01)04035459407045/ Order #s 877130 871608 869477 873755 873408 873462 872532 871154 880168 880929 865865 873716 866700 870221 871517 875929 877106 877351 871959 875613 866847 882306 881541 869191 869393 875444 872004 867991 880396 868574 877787 876488 879697 866838 875675 877656 867391 873489 869196 872232 870921 867678 868728 877709 867990 879513 869349 869864 880431 879922 882026 872429 876236 871997 881374 880275 876177 869274 870606 879926 871392 878189 869601 867903 876762 867908 867780 873752 867175 872533 879230; REF: 17V2030/UDI: (01)04035459407038/ Order #s: 873689 877130 873755 873462 872532 880168 877383 881065 865865 873716 871519 875929 867520 875141 875160 867907 874430 879427 877351 875613 866847 871613 873697 874810 875444 879594 882000 867991 880396 880970 868574 868353 876488 866838 867391 873489 873231 869196 872232 876230 870921 867678 873227 877571 868728 877709 879513 869864 876395 880173 869459 872429 869390 868305 876236 880312 871997 881374 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: completed.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0671-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.