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Townsend Design recalls

Townsend Design has 3 recalls on record with the FDA and USDA, the earliest in 2024 and the latest reported on 17 Jan 2024. The most frequent reason is device malfunction.

Total recalls3since 2024

Last 12 months0reported

Class I00% of total

Ongoing0latest 17 Jan 2024

Recalls per month, last 24 months

click a bar for that month

0Oct '24 0 0 0Jan '25 0 0 0Apr 0 0 0Jul 0 0 0Oct 0 0 0Jan '26 0 0 0Apr 0 0 0Jul 0 0

Severity split

Class I 0 0%Class II 3 100%Class III 0 0%

Why townsend design is recalled

Device Malfunction3100%

Product types

Other Medical Devices3100%

By year

20243100%

All townsend design recalls, newest first

3 total

Reported	Class	Recall	Company	Reason	Where
17 Jan 2024Device	CLASS II	Sprystep Vector, Custom made device dynamic ankle-foot recalled	Townsend Design	Device Malfunction	41 states
17 Jan 2024Device	CLASS II	Custom Sprystep, custom made device dynamic ankle-foot recalled	Townsend Design	Device Malfunction	41 states
17 Jan 2024Device	CLASS II	Sprystep Vector Kafo, Custom made device dynamic ankle-foot recalled	Townsend Design	Device Malfunction	41 states

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.