MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2018-10-11 for ISOFLEX 35X84 DARTEX W/FB 2800000000 manufactured by Stryker Medical-kalamazoo.
[123359765]
The customer reported a general increase in pressure injuries. No specific incidents were reported.
Patient Sequence No: 1, Text Type: D, B5
[134206778]
Investigation determined the complaint was entered with an incorrect product. The product is not manufactured by stryker. Hill-rom, the manufacturer is responsible for all regulatory reporting and complaint handling and closure. This complaint was sent to hill-rom for regulatory reporting determination.
Patient Sequence No: 1, Text Type: N, H10
[134206779]
The customer reported a general increase in pressure injuries. No specific incidents were reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 0001831750-2018-01088 |
| MDR Report Key | 7955427 |
| Report Source | USER FACILITY |
| Date Received | 2018-10-11 |
| Date of Report | 2019-01-14 |
| Date of Event | 2018-09-14 |
| Date Mfgr Received | 2018-09-14 |
| Date Added to Maude | 2018-10-11 |
| 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 | ISOFLEX 35X84 DARTEX W/FB |
| Generic Name | BED, FLOTATION THERAPY, POWERED |
| Product Code | IOQ |
| Date Received | 2018-10-11 |
| Catalog Number | 2800000000 |
| Device Availability | Y |
| Device Age | DA |
| 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 | 2018-10-11 |