MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-01-25 for ISOLIBRIUM SUPPORT SURFACE - D 2972000000 manufactured by Stryker Medical-kalamazoo.
[134190337]
This mdr is part of the fda voluntary malfunction summary reporting program. The device was not evaluated; the issue was reported by the customer, but they did not require an evaluation as no product malfunction/defect is alleged. There was no remedial action taken. This device is not labeled for single use.
Patient Sequence No: 1, Text Type: N, H10
[134190338]
This report summarizes 1 malfunction event, where it was reported it was difficult to perform x-rays with the mattress. There was patient involvement, however there were no consequences or impacts to the patient.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0001831750-2019-00025 |
MDR Report Key | 8279085 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2019-01-25 |
Date of Report | 2019-01-25 |
Date of Event | 2018-10-01 |
Date Mfgr Received | 2019-01-01 |
Date Added to Maude | 2019-01-25 |
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 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. MARY KLAVER |
Manufacturer Street | 3800 EAST CENTRE AVENUE |
Manufacturer City | PORTAGE MI 49002 |
Manufacturer Country | US |
Manufacturer Postal | 49002 |
Manufacturer Phone | 2693292100 |
Manufacturer G1 | STRYKER MEDICAL-KALAMAZOO |
Manufacturer Street | 3800 EAST CENTRE AVENUE |
Manufacturer City | PORTAGE MI 49002 |
Manufacturer Country | US |
Manufacturer Postal Code | 49002 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ISOLIBRIUM SUPPORT SURFACE - D |
Generic Name | BED, PATIENT ROTATION, POWERED |
Product Code | IKZ |
Date Received | 2019-01-25 |
Catalog Number | 2972000000 |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | STRYKER MEDICAL-KALAMAZOO |
Manufacturer Address | 3800 EAST CENTRE AVENUE PORTAGE MI 49002 US 49002 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-01-25 |