SPRYSTEP VECTOR — Class II medical device recall Z-0671-2024
Completed recall by Townsend Design, reported 2024-01-17, distributed in AL, AR, AZ, CA, CO, CT, DC, DE…. Due to potential air pockets between layers of material, their is the potential for complete struct breakage o
| Recall number | Z-0671-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Completed |
| Voluntary or mandated | Voluntary |
| Recalling firm | Townsend Design, Bakersfield, CA, United States |
| Recall initiated | 2023-09-23 |
| Classified | 2024-01-05 |
| Reported by FDA | 2024-01-17 |
| Distributed | 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 |
| Countries outside the US | AU, CA, GB, JP, NL, NZ |
| Quantity | 898 units |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 04035459407038, 04035459407045, 04035459407052, 04035459407069, 04035459407076, 04035459407083, 04035459407090, 04035459407106, 04035459414500, 04035459414517, 04035459414524, 04035459414531, 04035459414548, 04035459414555 |
| Model numbers | 17V1030, 17V1031, 17V1032, 17V1033, 17V1035, 17V1036, 17V1037, 17V2030, 17V2031, 17V2032, 17V2033, 17V2035, 17V2036, 17V2037 |
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 for recall
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0671-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.