MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-10-10 for STRYKER 40100410 manufactured by Stryker.
[3072628]
While using a power saw in the left wrist, small pieces of the saw blade broke off. The blade was a wright blade #(b)(4) on our stryker tps.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5027242 |
| MDR Report Key | 2792464 |
| Date Received | 2012-10-10 |
| Date of Report | 2012-10-10 |
| Date of Event | 2012-08-09 |
| Date Added to Maude | 2012-10-17 |
| Event Key | 0 |
| Report Source Code | Voluntary 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 | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | STRYKER |
| Generic Name | WRIGHT BLADE |
| Product Code | EMF |
| Date Received | 2012-10-10 |
| Model Number | 40100410 |
| Lot Number | UNK |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | STRYKER |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-10-10 |