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Terminated

Invacare Lynx and Panther Scooters, motorized 3-wheeled vehicles.

FDA Recall Z-0574-03 · Posted 2003-02-25

Recalling FirmInvacare Corp
Recall StatusTerminated
Product CodeITI
Date Initiated2003-02-10
Date Terminated2012-04-12
Product Quantity5,029 scooters

Reason for Recall

A short circuit within the charger harness may cause heat damage to the units with potential for fire.

Firm Action

On 3/10/2003, the firm mailed recall letters to all affected dealer accounts. The dealers were asked to contact all customers who have purchased the scooters.

Root Cause

Other

Distribution Pattern

The scooters were shipped to dealerships located nationwide, and to foreign distributors located in Barbados, Argentina, Isreal, and Bermuda.

Related FDA 510(k) Records

Devices referenced by this recall via K-numbers.

K010135MODELS LYNX AND PANTHER MOTORIZED SCOOTERS, MODELS LYNX SX-3, LYNX SX-3P, LYNX LX-3, LYNX LX-3, PANTHER LX-4Invacare Corp. · 2001-02-16

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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