MAUDE Adverse Event Report: DOLOMITE AB DOLOMITE MAXI ROLLATOR 550 7331492560448; WALKER, MECHANICAL

Model Number 12070-43-21M

Device Problem Component Missing (2306)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 02/19/2015

Event Type  malfunction  

Event Description

The walker lost a wheel during a walk outside, when walking on uneven surfaces outside the public swimming bath.The user managed to remain standing.

Manufacturer Narrative

(b)(4).No injury alleged.Malfunction alleged.Mdr filed with the fda the walker lose a wheel during a walk outside.When walking on uneven surfaces outside the public swimming bath.The user managed to remain standing.The futura is the same /similar to a product or products which are, or have been manufactured and/or marketed by invacare in u.S.The incident occured in (b)(6) on a device marketed by invacare (b)(4).

• Brand Name: DOLOMITE MAXI ROLLATOR 550 7331492560448
• Type of Device: WALKER, MECHANICAL
• Manufacturer (Section D): DOLOMITE AB; vaxjovagen 303; dio ; SW
• Manufacturer (Section G): DOLOMITE AB; vaxjovagen 303; dio ; SW
• Manufacturer Contact: kevin guyton ; one invacare way; elyria, OH 44035 ; 8003336900
• MDR Report Key: 4732947
• MDR Text Key: 5707249
• Report Number: 9615290-2015-00174
• Device Sequence Number: 1
• Product Code: ITJ
• Combination Product (y/n): N
• Reporter Country Code: SW
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Medical Equipment Company Technician/Representative
• Type of Report: Initial
• Report Date: 03/30/2015

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Lay User/Patient
• Device Model Number: 12070-43-21M
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 03/30/2015
• Initial Date FDA Received: 04/28/2015
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1
• Patient Outcome(s): Other