FDA Adverse Event Injury Summary report: N

130 ACORN T700 RH USA

MDR report key: 15175420 · Received August 5, 2022

Report

Report Number
3003124453-2022-00008
Event Type
Injury
Date Received
August 5, 2022
Date of Event
December 2, 2021
Report Date
August 5, 2022
Manufacturer
ACORN STAIRLIFTS, INC.
Product Code
PCD
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

ATTACHMENTS: INVESTIGATION REPORT, WORK COMPLETION REPORT.

Description of Event or Problem · 0

ON (B)(6) 2021. THE CUSTOMER CONTACTED ACORN STAIRLIFTS, INC. (ACORN) BECAUSE THE UPPER SAFETY COVER ON THE STAIRLIFT WAS LOOSE. ON (B)(6) 2021, THE CUSTOMER CONTACTED ACORN TO COMMUNICATE HAT HIS WIFE HAD FALLEN USING THE STAIRS. SPECIFICALLY, THE INCIDENT OCCURRED ON (B)(6) 2021 AFTER HE CONTACTED ACORN ABOUT THE SAFETY COVER BEING LOOSE. HIS ACCOUNT IS THAT HIS WIFE WAS WALKING DOWN THE STAIRS, SHE FELL AND SHE WAS WEDGED UNDER THE RAIL RESULTING IN STITCHES IN BOTH ARMS, BOTH KNEES AND HER LEFT HIP. THE CUSTOMER DID CLAIM THAT THE STAIRLIFT WAS NOT WORKING AT THE TIME OF THE INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2603179 130 ACORN T700 RH USA POWERED STAIRWAY CHAIR LIFT PCD ACORN STAIRLIFTS, INC. 130 T700 RH

Patients

Seq Age Sex Outcome Treatment
1 76 YR Female Other| R