Facility

WW-West

1 recall(s) on record — most severe on record: Class II.

Key facts

1recalls · worst Class II

—inspections in our data

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3035765256
Establishment type	Manufacture Medical Device
Location	8743 E Pecos Rd Mesa, AZ, US 85212
Registration status	Active · expires 2026
Parent company	WillowWood Global LLC (owner-operator 1522166)
Brand names	Prosthetic Foot/Ankle, multiple; Single Axis; Impulse; SACH; Meta Shock; Meta Arc; Meta Shock X; KOA LP; Meta Core; META Flow

Activity by year

Recalls (1)

Devices registered here (1)

Component, External, Limb, Ankle/Foot
Product code ISH (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3420

Recalls & enforcement

Class IIOngoing2021-04-20
the firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was used in place of the 5/8 pin. Over time, the shorter pin may not engage in either the upper or lower body, causing the cord to come loose or slip which could result in the loss of suspension.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “WW-West (FEI 3035765256) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3035765256-ww-west/

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