MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-17 for KONIG METZENBAUM SCISSORS MDS0828318 manufactured by Medline Industries Inc..
[175395126]
Metzenbaum scissors failed while in use on patient. All pieces recovered. Two handles, one screw, and broken scissor tip.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 9601172 |
| MDR Report Key | 9601172 |
| Date Received | 2020-01-17 |
| Date of Report | 2020-01-08 |
| Date of Event | 2020-01-03 |
| Report Date | 2020-01-08 |
| Date Reported to FDA | 2020-01-08 |
| Date Reported to Mfgr | 2020-01-17 |
| Date Added to Maude | 2020-01-17 |
| 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 | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | KONIG METZENBAUM SCISSORS |
| Generic Name | SCISSORS, GENERAL, SURGICAL |
| Product Code | LRW |
| Date Received | 2020-01-17 |
| Catalog Number | MDS0828318 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDLINE INDUSTRIES INC. |
| Manufacturer Address | THREE LAKES DRIVE NORTHFIELD IL 60093 US 60093 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-01-17 |