MAXI MOVE KMCLUN

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-02-25 for MAXI MOVE KMCLUN manufactured by Arjohuntleigh Magog Inc..

Event Text Entries

[188483906] The arjo representative was informed about the event related to maxi move device. It was reported that the resident was transferred from a chair to the bed. When the caregiver tried to tilt the resident to the sitting position the powered dps was not working. Due to this fact the caregiver decided to placed the resident back into the chair. During transferring the resident got twisted sideways in the sling and the caregiver got the power dps working again. The resident's leg got twisted resulting in the injury. Resident sustained a knee injury and fracture. The orthopedic surgeon applied a soft cast to immobilize the knee. This resident had osteopenia.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1419652-2020-00015
MDR Report Key9749449
Date Received2020-02-25
Date of Report2020-02-25
Date of Event2019-12-31
Date Facility Aware2020-01-28
Report Date2020-02-25
Date Reported to FDA2020-02-25
Date Reported to Mfgr2020-02-25
Date Added to Maude2020-02-25
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAXI MOVE
Generic NameLIFT, PATIENT, NON-AC-POWERED
Product CodeFSA
Date Received2020-02-25
Model NumberKMCLUN
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerARJOHUNTLEIGH MAGOG INC.
Manufacturer Address2001 TANGUAY STREET MAGOG, QUEBEC J1X 5Y5 CA J1X 5Y5


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-02-25

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