Townsend Design recalls SPRYSTEP VECTOR custom ankle-foot orthoses with reference numbers 17V1030-17V2037 due to potential air pockets causing complete structural breakage.
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
Townsend Design is recalling SPRYSTEP VECTOR custom ankle-foot orthoses (AFOs) because air pockets between layers could cause the device to completely break. This poses a risk of injury if the device fails during use.
The device may develop air pockets between its layers, which can lead to complete structural failure. If the device breaks while in use, it could cause injury or loss of support for the user.
Individuals who own or use the recalled SPRYSTEP VECTOR AFOs with reference numbers 17V1030 through 17V2037 are affected. People with mobility impairments who rely on these devices for support are at higher risk.
Check for reference numbers 17V1030 to 17V2037 on the device or order history. The product is a custom-made dynamic ankle-foot orthosis (AFO) used for mobility support.
Look for reference numbers 17V1030 through 17V2037 on the device or order history.
Reach out to Townsend Design directly for further instructions on how to address the issue.
The devices may develop air pockets between layers, which can cause complete structural breakage during use.
Check for reference numbers 17V1030 through 17V2037 on the device or order history.
Contact Townsend Design directly for further instructions on how to address the issue.
We’ve drafted a message you can send Townsend Design to request your refund or repair — edit it as you like.
Subject: Recall Z-0671-2024 — Townsend Design Townsend Design Hello, I own a Townsend Design that is covered by recall Z-0671-2024 from Townsend Design. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
