HOVERMATT

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-08-10 for HOVERMATT manufactured by Hovertech/ D.t. Davis Enterprise Ltd..

Event Text Entries

[82678063] My (b)(6) father who is a wwii disabled veteran was severely injured during a normal day surgery at (b)(6) hospital by hospital staff not knowing the correct way to use a product called the hovermatte and the harm was intensified because of a faulty iv. The hospitalist and internal medicine doctors i believe at this hospital are quite good at creating almost a 3 stooges act to cover up their negligence. I will attach pictures and the letter sent to the joint commission on my complaints. They covered their bases by masking the places that were either bruises or burns by allowing nurses to use topical creams for one diagnosis when i believe they knew what happened and were covering it up.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5071528
MDR Report Key6791312
Date Received2017-08-10
Date of Report2017-08-10
Date of Event2017-06-30
Date Added to Maude2017-08-14
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPATIENT FAMILY MEMBER OR FRIEND
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameHOVERMATT
Generic NameHOVERMATT
Product CodeFRZ
Date Received2017-08-10
Device AvailabilityY
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerHOVERTECH/ D.T. DAVIS ENTERPRISE LTD.


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Life Threatening; 3. Other; 4. Required No Informationntervention; 5. Deathisabilit 2017-08-10

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