MAUDE Adverse Event Report: ZHONGSHAN BLISS MEDICAL DRIVE DEVILBIOSS HEALTHCARE; WALKER, MECHANICAL

Model Number	10210-4ASM
Medical Device Problem Code	Mechanical Problem (1384)
Health Effect - Clinical Code	Bone Fracture(s) (1870)
Date of Event	12/15/2024
Type of Reportable Event	Serious Injury
Event or Problem Description
Drive devilbiss healthcare was notified of an incident involving a walker by the end user, who reported that the back right leg bent, causing her to fall and sustain a fractured heel and bruising.Inspection of the device confirmed that the leg was bent.As part of its complaint review and evaluation process, drive devilbiss healthcare will also notify the manufacturer of the product about this complaint.

• Brand Name: DRIVE DEVILBIOSS HEALTHCARE
• Common Device Name: WALKER, MECHANICAL
• Manufacturer (Section D): ZHONGSHAN BLISS MEDICAL; no.98, dongshengzhen; zhaoyi road; zhongshan, guangdong 52841 4; CH 528414
• MDR Report Key: 21265674
• Report Number: 2438477-2025-00008
• Device Sequence Number: 4275972
• Product Code: ITJ
• UDI-Device Identifier: 00822383226200
• UDI-Public: (01)00822383226200
• Combination Product (Y/N): N
• Initial Reporter State: MD
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Importer
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 01/29/2025
• Report Date (Section F): 01/29/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Lay User/Patient
• Device Model Number: 10210-4ASM
• Device Catalogue Number: 10210-4ASM
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/08/2025
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 01/02/2025
• Event Location: Home
• Date Report to Manufacturer: 01/29/2025
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 01/29/2025
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 66 YR
• Patient Sex: Female
• Date Report Sent to FDA: 01/29/2025