Recall events
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Event 93299
Event summary
Timeline bucket September 23, 2023
Product types Device
Classifications Class II
Statuses Completed
Recalling firm wording Townsend Design
Dossier provenance
Source snapshots represented here
openFDA Device Enforcement
Report-date coverage
June 20, 2012–July 08, 2026
Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
openFDA Device Recall
event_date_initiated coverage
June 01, 1997–June 30, 2026
Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.
How coverage and grouping work
Complete imported group
Every recalled product in this event
3 official enforcement rows
Product dates, classifications, firms, and source wording remain attached to their individual rows.
Opening this dossier never hides products that did not match a prior timeline filter.
device · product 1 of 3
CUSTOM SPRYSTEP, custom made device dynamic ankle-foot orthosis (AFO) , Ref #s: 17C1000, 17C2000, 17C1010, 17C2010, 17C1040, 17C2040
Z-0670-2024
Recall number Z-0670-2024
Initiated September 23, 2023
Classification Class II
Status Completed
Quantity 248 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0670-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[52332]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
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.
Code information REF: 17C1000: UDI: (01)04035459406987/Order #s: 875138 873876 870246 878309 870876 867906 867207 874519 870238 872326 880231 877998 881515 876713 873527 865318 872900 879715 871401 876266 869208 878409 872012 881081 876737 873872 873873 873874 881432 879731 869605 870645 872295 877649 880838 871165 881042 867389 872007 879027 872785 876112 876597 869483 876193 881451 872018 869463 879627 874007 877229 873391 871394 872322 879239 880900 878438 878984 869479 866311; REF:17C2000: UDI: (01)04035459406970/Order #s: 877272 873876 878309 870876 878859 870238 872332 881515 865113 871377 873527 865318 872900 876830 879719 876266 869208 878409 879736 877464 881087 876758 882039 881432 868575 869605 870239 880069 881858 881004 871167 877863 879027 872785 876112 872231 867679 867192 869483 874204 871980 872018 869463 876197 874007 877229 877657 877032 877686 878973 871394 878061 877487 873224 879239 878438 878984 881309 869479 869481 867818 881671; REF: 17C1010: UDI: (01)04035459407021/Order #s: 870369 881820 874040 879520 876180 870245 876186 871950 867672 878203 879246 880392 867984 879241 869603 877984 868694 876481 872772 869860 872009 869189 877643 874640 880427 867373 872516 869542 877296 870860 877502 867305 879052 878973 881513 865708 873091 879253; REF:17C2010: UDI: (01)04035459407014/Order #s: 868833 881820 877376 874040 879520 876180 869636 876186 869607 867672 878203 879246 880212 867984 869391 878893 875114 881605 868694 874706 869860 877648 874640 867373 867171 872516 877296 870860 877502 867305 879052 873091 879253 874211; REF:17C1040: UDI: (01)04035459407007/Order #s: 871643 871906 878303 869612 872321 872024 874230 876323 880348 878814 878816 871550 875852 880935 879597 880879 881558 875414 879602 880582 869590 869377 869013 872941 871638 870777; REF:17C2040:UDI: (01)04035459406994/Order #s: 871407 878303 874794 872024 877715 867407 868726 880348 878814 878816 873386 877977 870640 878844 875126 880315 871164 881558 878181 870868 869377 869389 869013 870919 870777 868615 871970 875970;
Distribution pattern US: AL AR AZ CA CO CT DC DE FL GA IA ID IL IN KENT KS KY LA MA MD ME MI MN MO MS MT NC NE NH NJ NM NV NY OH OK OR PA QC SC SD TN TX UT VA VT WA WI WV WY, Puerto Rico, OUS: None OUS: Canada, New Zealand, Japan, Australia, Netherlands, United Kingdom
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[37497]
FDA event record
· Exact recall-number query on openFDA
device · product 2 of 3
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
Z-0671-2024
Recall number Z-0671-2024
Initiated September 23, 2023
Classification Class II
Status Completed
Quantity 898 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0671-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[16826]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
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.
Code information 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 869931 870606 875391 876579 867903 876762 881372 872533 873878 879230; Ref: 17V1031/UDI: (01)04035459407069/ Order #s: 869376 877592 868548 876410 878842 881809 880881 877660 876614 882052 879617 872834 882487 878021 879707 885211 873387 876483 869443 870617 879042 880962 872482 878416 880911 866671 869932 875859 879015 879025 879592 880159 880964 876760 879612 880877 871624 866854 880364 869861 878403 871982 873934 881784 875842 879494 871626 881116 871383 880615 867163 880906 873012 879916 872027 874269 879786 869348 869509 877134 868540 869454 870916 877470 869449 870345 876431 879886 869492 871615 871474 871983 874858 870224 880370 875734 879805 884301 877916 875650 881023 870863 881420 870976 881627 871168 873674 873378 873382 874252 880193 877172 871371 881427 879725 873968 875137 880850 881995 872026 871100 874324 878077 879796 880217 873603; REF: 17V2031/UDI: (01)04035459407052/Order #s: 870883 869376 877592 876410 878842 876357 876638 866839 880881 877660 874924 867409 878010 879617 879707 885211 873387 876483 876836 869443 869362 879042 880962 871162 872482 878416 880911 866894 869932 875785 875790 875859 877250 877652 877654 880159 879612 879010 880364 878403 871982 881116 871383 879233 880906 873012 879916 879786 869348 877134 871942 868540 877470 874106 869449 870345 869395 869924 869492 871615 871983 871995 874858 870224 880370 875734 879805 884301 877916 877468 875650 877190 881023 870863 871391 870976 873518 881627 871168 873674 869351 869462 867319 874252 871225 880193 871371 872380 875375 871947 882233 877731 875137 881995 867753 862493 871100 873189 866988 876363 880217 873603; REF: 17V1032/UDI:(01)04035459407083/Order #s: 879043 871155 869394 870244 868306 869846 873447 873150 881441 878461 870616 869193 880166 879026 875477 872812 871999 869456 880378 882237 873163 866891 881632 873875 870072 871148 882041 866674 869923 871636 877108 873672 873563 878342 872015 876569 870596 870241 870870 880390 878795 879729 868544 875802 877375 869095 869379 875805 879228 879735 873688 866979 873526 875481 880184 881636 878420 872220 882084 873218 876845 878766 877986 873395 875980 869882; REF: 17V2032/UDI:(01)04035459407076/Order #s: 878742 879043 871155 875669 870618 868306 866984 872243 873447 876723 869611 877298 868547 873150 871533 872219 878461 867665 880166 880281 869857 872812 871999 880378 882220 879024 866891 877985 868946 876783 870072 871148 877701 874254 869387 874099 877069 878255 868825 881401 872015 876569 870596 866660 867675 869205 870240 870865 877578 872517 878795 866983 869329 871975 879005 873670 867673 873751 873698 873750 869095 870862 866979 873526 881636 868303 877491 872220 873218 876845 873753 878766 874799 873395 869882 879739; REF: 17V1033/UDI: (01)04035459407106 /Order #s: 879768 866975 877097 868839 873466 873690 876718 879809 873879 869591 868552 869280 870602 873397 869327 867997 872221 878458 872814 881020 869198 880565 870603 868000 869382 871273 877474 883394 878014 868870 880691 869200 874878 872788 868299 869926 877131 881398 875737 877612 872816 870219 871943 870210 868140 870223 873671 876904 869805 881537 877720 871946 870918 880357 871390 873390 876912 877039 867912 878390 866282 866824; REF:17V2033/UDI: (01)04035459407090/Order #s: 870990 867910 875146 873690 869883 879812 879809 869591 878290 874221 869613 869637 871639 867390 876464 880418 870600 880262 869191 873392 880034 869382 869082 877787 880242 880257 866851 874731 878002 878006 866982 873708 866673 869445 877131 881398 879883 875737 872816 870219 868543 881046 877846 876568 876904 875059 869805 878989 881537 877720 871946 878170 881016 876203 879235 882033 867758 879983 873241; REF:17V1035/UDI: (01)04035459414517 /Order #s: 875828 872283 871945 877520; REF: 17V2035/UDI: (01)04035459414500/Order #s: 877598 873877 879077 872285; REF:17V1036/UDI: (01)04035459414531/Order #s: 871151 873211 875154 878812 874332 882211 882220 882227 872002 877102 876353 874436 877407 877650 872952 880160 877588; REF:17V2036/UDI: (01)04035459414524/Order #s: 871151 876733 869846 879479 875154 878812 874332 871978 882211 882227 880870 872002 876353 872229 873703 877650 877990 873702 877588; REF: 17V1037/UDI:(01)04035459414555/Order #s: 881380, 878083; REF: 17V2037/UDI:(01)04035459414548/Order #s: 881380, 878083
Distribution pattern US: AL AR AZ CA CO CT DC DE FL GA IA ID IL IN KENT KS KY LA MA MD ME MI MN MO MS MT NC NE NH NJ NM NV NY OH OK OR PA QC SC SD TN TX UT VA VT WA WI WV WY, Puerto Rico, OUS: None OUS: Canada, New Zealand, Japan, Australia, Netherlands, United Kingdom
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38078]
FDA event record
· Exact recall-number query on openFDA
device · product 3 of 3
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
Z-0672-2024
Recall number Z-0672-2024
Initiated September 23, 2023
Classification Class II
Status Completed
Quantity 334 units
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
These labels are deterministic app interpretations, not FDA categories.
Official device-enrichment evidence · Sourced
Process control
Enrichment source openFDA Device Recall
Exact join Official recall number Z-0672-2024
Source locator 0001-device-recall-0001-of-0001.json.zip#results[5082]
Snapshot SHA-256 77e96a0ce750de9fa4bb4737d40b653784372b5abe88b9de499ad51edd808a4b
Open official device record
Compare all device evidence states
Inspect official wording and provenance
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.
Code information 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 874242 876221 876221 874239 877527 868310 864590 872312 872312 874217 874217 875682 875682 875682 875682 865743 864949 864949 864960 872833 872535 872535 870881 870881 875053 875053 877459 866653 876099 870214 873791 873025 863340 866810 868042 868534 869716 871539 874028 877634 865745 876675 872003 873863 874082 875898 873401 878664 871403 872028 865207 870243 873579 874453 874453 867886 878116 867382 871008 878134 865464 865464 867932 872463 872463 876902 876902 868831 869045 867147 865504 872823 871992 875377 871991 877676 877676 867685 866669 864414 879749 874886 868285 877400 851811 872744 867952 874200 879006 863770 867434 868553 868553 872288 878683 870549 870549 880814 869364 869364 873639 866843 866843 874962 867157 874203 877228 869368 877671 865110 877397 876724 876724 868568 874257 879001 869360 874434 865199 869355 869357 872782 872782 876495 878215 867953 877996 877996 865741 873810 877262 877262 866658 869190 865352 866846 866846 877116 877116 869120 881824 872223 868495 868495 879817 877705 868571 864955 869325 872022 876058 876506 865502 867369 871309 877674 873159 865734 874271 873186 873186 877902 871616 875378 879484 871718 873403 877625 877625 868835 872314 866526 866598 867787 868609 872580 872926 873740 873740 874952 875239 875239 878620 878914 867143 878743 875178 873923 870027 877741 867148 870660 877200 865435 864078 879739 877273 878832 878832 873169 865102 874535
Distribution pattern US: AL AR AZ CA CO CT DC DE FL GA IA ID IL IN KENT KS KY LA MA MD ME MI MN MO MS MT NC NE NH NJ NM NV NY OH OK OR PA QC SC SD TN TX UT VA VT WA WI WV WY, Puerto Rico, OUS: None OUS: Canada, New Zealand, Japan, Australia, Netherlands, United Kingdom
Official fact provenance
Dataset openFDA Device Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 1c273507f2e0fc8c5b330c3716a1392933bd90a42a460afcb7368f298d5cbd3a
Raw source locator 0001-device-enforcement-0001-of-0001.json.zip#results[38105]
FDA event record
· Exact recall-number query on openFDA