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..
[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
Report Number | MW5071528 |
MDR Report Key | 6791312 |
Date Received | 2017-08-10 |
Date of Report | 2017-08-10 |
Date of Event | 2017-06-30 |
Date Added to Maude | 2017-08-14 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | PATIENT FAMILY MEMBER OR FRIEND |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | HOVERMATT |
Generic Name | HOVERMATT |
Product Code | FRZ |
Date Received | 2017-08-10 |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | HOVERTECH/ D.T. DAVIS ENTERPRISE LTD. |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization; 2. Life Threatening; 3. Other; 4. Required No Informationntervention; 5. Deathisabilit | 2017-08-10 |