Townsend Design 2024-01-17 Health serious FDA
Health · FDA · Recall #FDA-Z-0672-2024
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking,… Recall
Issued January 17, 2024 · Townsend Design
In January 2024, Townsend Design recalled the SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
What you should do
- 1 Stop using SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Townsend Design to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Townsend Design
- Category
- Health
- Recall date
- January 17, 2024
- Units affected
- Not reported
- Sold at
- 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
- Recall number
- FDA-Z-0672-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Townsend Design has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.