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CTM Mobility Scooter

C.T.M. HOMECARE PRODUCT, INC. · Model HS-580 · UDI-DI 00852202007208

INI

510(k) clearances

2,715

Adverse events (74 deaths)

Recalls

Facilities

Description

Mid-Range Four Wheel Mobility Scooter, Red/Blue/Silver

Recalls

Date	Firm	Reason
2021-04-01	Merits Holdings Co. dba Merits Health Products, Inc.	Seat baseplate pin has broken in the field.
2014-01-21	Golden Technologies, Inc.	Buzzaround XL scooters' front to rear lockup can become unintentionally disengaged due to possible improper fit of the front alignment cup to the rear alignment screw.
2013-09-27	S.A.E. AFIKIM	Breeze C Scooter, motorized 3-wheeled electric scooter for elderly people, is recalled because it may become unresponsive during operation due to an electrical contact which may fa
2011-12-07	Invacare Corporation	Invacare Corporation decided to recall the products because the scooter backrest fails unexpectedly due to seat flexing, and this has the potential to result in a consumer falling
2011-06-22	Pride Mobility Products Corp	Contract manufacturer error. Component part(s) (fuses) specifications were not adhered to as outlined in Pride's Engineering drawings.
2011-06-22	Pride Mobility Products Corp	Contract manufacturer error. Component part(s) (fuses) specifications were not adhered to as outlined in Pride's Engineering drawings.
2010-11-26	Pride Mobility Products Corp	The main harness connector was manufactured without the required back shield sealing protection. As a result, there is the potential for water to seep through the nonconforming har
2010-09-27	Electric Mobility Corp	Scooter seat bases were found to have insufficient welding which may lead to the seat base becoming loose and causing the seat to wobble. This may result in complete failure of the
2010-09-27	Electric Mobility Corp	Scooter seat bases were found to have insufficient welding which may lead to the seat base becoming loose and causing the seat to wobble. This may result in complete failure of the
2010-09-27	Electric Mobility Corp	Scooter seat bases were found to have insufficient welding which may lead to the seat base becoming loose and causing the seat to wobble. This may result in complete failure of the

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.