MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-11-27 for * UNK manufactured by Stryker Corporation.
| Report Number | 3591559 |
| MDR Report Key | 3591559 |
| Date Received | 2013-11-27 |
| Date of Report | 2013-11-27 |
| Date of Event | 2013-02-22 |
| Report Date | 2013-11-27 |
| Date Reported to FDA | 2013-11-27 |
| Date Reported to Mfgr | 2014-01-23 |
| Date Added to Maude | 2014-01-24 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| 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 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | * |
| Generic Name | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
| Product Code | DWI |
| Date Received | 2013-11-27 |
| Model Number | UNK |
| Catalog Number | UNK |
| Lot Number | UNK |
| ID Number | * |
| Operator | PHYSICIAN |
| Device Availability | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER CORPORATION |
| Manufacturer Address | 4100 EAST MILHAM AVE KALAMAZOO MI 49001 US 49001 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2013-11-27 |