# FDA recall Z-0672-2024

> **Townsend Design** · Class II · device recall initiated 2023-09-23.

## Product

SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

## 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.

## Distribution

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

## Key facts

- **Recall number:** Z-0672-2024
- **Recalling firm:** Townsend Design
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2023-09-23
- **Report date:** 2024-01-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Bakersfield, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0672-2024

## Citation

> AI Analytics. FDA recall Z-0672-2024. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0672-2024. Source: US FDA. Licensed CC0.

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