MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-10-14 for FOAM MATTRESS VINYL 9153633137 IES0080 manufactured by Invacare (ltd) Uk.
[28510546]
Should additional information become available for the patient a supplemental record will be filed.
Patient Sequence No: 1, Text Type: N, H10
[28510547]
Dealer is stating that the mattress has a sink hole in the middle.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3007582653-2015-00009 |
MDR Report Key | 5146816 |
Date Received | 2015-10-14 |
Date of Report | 2015-09-17 |
Date Mfgr Received | 2015-09-17 |
Date Added to Maude | 2015-10-14 |
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 | 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 (LTD) UK |
Manufacturer Street | PENCOED TECHNOLOGY PARK PENCOED |
Manufacturer City | BRIDGEND |
Manufacturer Country | UK |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | FOAM MATTRESS VINYL 9153633137 |
Generic Name | CUSHION, FLOTATION |
Product Code | KIC |
Date Received | 2015-10-14 |
Model Number | IES0080 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INVACARE (LTD) UK |
Manufacturer Address | PENCOED TECHNOLOGY PARK PENCOED BRIDGEND UK |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-10-14 |