MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2015-01-23 for INVACARE PROPEL BACK 16 IN WIDE PCPROPEL manufactured by Invacare Cleveland Street.
[5393885]
It has been reported by a provider that over time, the bolts came loose on a propel back, and the bracket that attaches to the back of the seating broke off.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1219590-2015-00026 |
MDR Report Key | 4448455 |
Report Source | 08 |
Date Received | 2015-01-23 |
Date of Report | 2015-01-16 |
Date Mfgr Received | 2015-01-16 |
Date Added to Maude | 2015-02-28 |
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 | MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | KEVIN GUYTON |
Manufacturer Street | ONE INVACARE WAY |
Manufacturer City | ELYRIA OH 44036 |
Manufacturer Country | US |
Manufacturer Postal | 44036 |
Manufacturer Phone | 8003336900 |
Manufacturer G1 | INVACARE CLEVELAND STREET |
Manufacturer Street | 899 CLEVELAND 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 | 3 |
Brand Name | INVACARE PROPEL BACK 16 IN WIDE |
Generic Name | CUSHION, WHEELCHAIR |
Product Code | KNN |
Date Received | 2015-01-23 |
Model Number | PCPROPEL |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INVACARE CLEVELAND STREET |
Manufacturer Address | 899 CLEVELAND STREET ELYRIA OH 44036 US 44036 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2015-01-23 |