Reported Jan 17, 2024 · Completed

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

Townsend Design

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Townsend Design · 4615 Shepard St · Bakersfield, CA · 93313-2339

Is this the product you have?

  • SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
Lot codes and dates
  • REF17VKCUS:UDI: /Order #s:

    94 of 94 codes

    • 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
  • REF17VKCUSX:
  • UDI/Order #s:

    240 of 240 codes

    • 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
    • 874242
    • 876221
    • 876221
    • 874239
    • 877527
    • 868310
    • 864590
    • 872312
    • 872312
    • 874217
    • 874217
    • 875682
    • 875682
    • 875682
    • 875682
    • 865743
    • 864949
    • 864949
    • 864960
    • 872833
    • 872535
    • 872535
Amount recalled
334 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

Why it was recalled

Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:33 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.