MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-11-06 for HTR5500 HTR-DELUXE MODEL 5500 9153635378 manufactured by Invacare Taylor Street.
[30879381]
Should additional information become available for the patient a supplemental record will be filed.
Patient Sequence No: 1, Text Type: N, H10
[30879382]
The right front caster is broken, seems bent.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1525712-2015-05268 |
MDR Report Key | 5207053 |
Date Received | 2015-11-06 |
Date of Report | 2015-10-16 |
Date Mfgr Received | 2015-10-16 |
Date Added to Maude | 2015-11-06 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
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 |
Manufacturer Contact | KEVIN GUYTON |
Manufacturer Street | ONE INVACARE WAY |
Manufacturer City | ELYRIA OH 44035 |
Manufacturer Country | US |
Manufacturer Postal | 44035 |
Manufacturer Phone | 8003336900 |
Manufacturer G1 | INVACARE TAYLOR STREET |
Manufacturer Street | 1200 TAYLOR STREET |
Manufacturer City | ELYRIA OH 44036 |
Manufacturer Country | US |
Manufacturer Postal Code | 44036 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | HTR5500 HTR-DELUXE MODEL 5500 9153635378 |
Generic Name | CHAIR AND TABLE, MEDICAL |
Product Code | KMN |
Date Received | 2015-11-06 |
Model Number | HTR5500 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INVACARE TAYLOR STREET |
Manufacturer Address | 1200 TAYLOR STREET ELYRIA OH 44036 US 44036 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-11-06 |