MAXI SKY 2

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-23 for MAXI SKY 2 manufactured by Arjohuntleigh Magog Inc..

Event Text Entries

[188580511] Collecting information is ongoing. Additional information will be provided upon investigation conclusion.
Patient Sequence No: 1, Text Type: N, H10


[188580512] It was reported that patient fell out of the device. Based on provided information it was possible that sling loop become detached from the device. As a consequence of the event patient sustained subdural hematoma.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9681684-2020-00022
MDR Report Key9864363
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2020-03-23
Date of Report2020-03-23
Date Added to Maude2020-03-23
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactKINGA STOLINSKA
Manufacturer StreetKS. WAWRZYNIAKA 2
Manufacturer CityKOMORNIKI 62-052
Manufacturer CountryPL
Manufacturer Postal62-052
Manufacturer Phone688282467
Manufacturer G1ARJOHUNTLEIGH MAGOG INC.
Manufacturer Street2001 TANGUAY STREET
Manufacturer CityMAGOG, QUEBEC J1X 5Y5
Manufacturer CountryCA
Manufacturer Postal CodeJ1X 5Y5
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMAXI SKY 2
Generic NameLIFT, PATIENT, NON-AC-POWERED
Product CodeFSA
Date Received2020-03-23
Device AvailabilityY
Device Eval'ed by MfgrY
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 2020-03-23

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