MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-01-04 for ISOFLEX 35X84 DARTEX W/FB 2800100000 manufactured by Stryker Medical-kalamazoo.
[132207591]
It was reported an end-of-life patient experienced a pressure injury while lying on the surface. The patient did not receive treatment for the injury, and was likely not rotated on the mattress, as they were end-of-life. No malfunction of the surface was reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 0001831750-2019-00001 |
MDR Report Key | 8217836 |
Date Received | 2019-01-04 |
Date of Report | 2019-01-04 |
Date of Event | 2018-12-06 |
Date Mfgr Received | 2018-12-06 |
Date Added to Maude | 2019-01-04 |
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. KRISTEN CANTER |
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 | 0 |
Brand Name | ISOFLEX 35X84 DARTEX W/FB |
Generic Name | BED, FLOTATION THERAPY, POWERED |
Product Code | IOQ |
Date Received | 2019-01-04 |
Catalog Number | 2800100000 |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
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 | 1. Other | 2019-01-04 |