MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2014-10-24 for BED, MANUAL 5310IVC manufactured by Invacare Florida Operations.
[20775380]
Dealer advised welds on bed frame are broken.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1031452-2014-15921 |
MDR Report Key | 4198551 |
Report Source | 08 |
Date Received | 2014-10-24 |
Date of Report | 2014-10-02 |
Date of Event | 2014-10-02 |
Date Mfgr Received | 2014-10-02 |
Date Added to Maude | 2014-11-06 |
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 | MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Contact | KAREN LOUGHREN |
Manufacturer Street | ONE INVACARE WAY |
Manufacturer City | ELYRIA OH 44035 |
Manufacturer Country | US |
Manufacturer Postal | 44035 |
Manufacturer Phone | 8003336900 |
Manufacturer G1 | INVACARE FLORIDA OPERATIONS |
Manufacturer Street | 2101 EAST LAKE MARY BLVD |
Manufacturer City | SANFORD FL 32773 |
Manufacturer Country | US |
Manufacturer Postal Code | 32773 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BED, MANUAL |
Generic Name | 880.5120 |
Product Code | FNJ |
Date Received | 2014-10-24 |
Model Number | 5310IVC |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INVACARE FLORIDA OPERATIONS |
Manufacturer Address | 2101 EAST LAKE MARY BLVD SANFORD FL 32773 US 32773 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2014-10-24 |