FDASeptember 23, 2023device
SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Due to potential air pockets between layers of material, their is the potential for complete struct breakage of knee-ankle-foot orthosis.
What to do
FDA enforcement status: Completed
Brands named
townsend designtownsend
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- CPSCCrate & Barrel Recalls Ana Dining Chairs Due to Fall Hazard2025-10-30
- CPSCIn Motion Design Recalls Evermore Surprise Eggs Due to Risk of Serious Injury; Violates Federal Lead Content Ban2025-10-02
- CPSCInnovative Designs Recalls Minecraft Light-Up Slap Ruler Bracelets Due to Risk of Serious Injury or Death from Button Cell Battery Ingestion Hazard; Violates Mandatory Standard for Toys2025-07-24
- CPSCCrate & Barrel Recalls Hampshire Cribs Due to Fall Hazard2024-04-25
- CPSCCascade Designs Recalls Camping Cooking Pots Due to Burn and Scald Hazards2024-02-22
- CPSCThe Museum of Modern Art Recalls Glass Little Wanderer Snow Globes Due to Laceration Hazard; Sold Exclusively at MoMA Design Stores2024-02-01
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