FDA Device recall Z-0672-2024

SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

FDA Device
Class II
completed
Published 2024-01-17

On 2024-01-17 the FDA classified a Class II recall of SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX 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-0672-2024
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 KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

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: 17VKCUS:UDI: /Order #s: 868003 864980 877514 867899 875411 875411 868308 871161 865211 881621 872534 881616 865744… REF: 17VKCUS:UDI: /Order #s: 868003 864980 877514 867899 875411 875411 868308 871161 865211 881621 872534 881616 865744 866309 876670 877270 864959 869294 868549 864957 864595 866551 866682 863308 875500 873400 865509 868828 875846 877677 869358 876200 873155 867381 878188 870222 870222 869927 873860 873860 865503 878668 878182 863772 866842 878791 865507 863707 872687 868289 873685 870922 870922 864367 865966 875463 871512 871512 870916 866919 879216 878252 879014 874428 867045 878412 863471 871544 874438 872200 870646 872512 865508 865508 876593 869370 865720 863470 876045 867371 865737 868736 873157 867694 875149 867457 875554 863353 867286 873781 873357 867357 873861 871137 REF: 17VKCUSX: UDI:/Order #s: 873093 877251 877251 864343 864343 876329 867359 867359 876421 867376 868295 863890 873575 868834 874561 874561 877602 877602 872207 872835 864342 867052 874879 878550 865056 865056 879221 877567 882074 871827 871827 865201 877909 877909 869372 869374 866576 867687 874

code_info

REF: 17VKCUS:UDI: /Order #s: 868003 864980 877514 867899 875411 875411 868308 871161 865211 881621 872534 881616 865744…

REF: 17VKCUS:UDI: /Order #s: 868003 864980 877514 867899 875411 875411 868308 871161 865211 881621 872534 881616 865744 866309 876670 877270 864959 869294 868549 864957 864595 866551 866682 863308 875500 873400 865509 868828 875846 877677 869358 876200 873155 867381 878188 870222 870222 869927 873860 873860 865503 878668 878182 863772 866842 878791 865507 863707 872687 868289 873685 870922 870922 864367 865966 875463 871512 871512 870916 866919 879216 878252 879014 874428 867045 878412 863471 871544 874438 872200 870646 872512 865508 865508 876593 869370 865720 863470 876045 867371 865737 868736 873157 867694 875149 867457 875554 863353 867286 873781 873357 867357 873861 871137 REF: 17VKCUSX: UDI:/Order #s: 873093 877251 877251 864343 864343 876329 867359 867359 876421 867376 868295 863890 873575 868834 874561 874561 877602 877602 872207 872835 864342 867052 874879 878550 865056 865056 879221 877567 882074 871827 871827 865201 877909 877909 869372 869374 866576 867687 874

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-0672-2024%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.