MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-03-12 for WECK manufactured by Pilling Weck.
[22046375]
#2 weck curette introduced into uterus during d&c. Curette was retrieved and noted to be missing loop end. Xray performed and foreign body not seen. Tip found in plastic gyn bag by circulating nurse.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5029367 |
| MDR Report Key | 3010675 |
| Date Received | 2013-03-12 |
| Date of Report | 2013-03-12 |
| Date of Event | 2013-03-11 |
| Date Added to Maude | 2013-03-20 |
| 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 |
| Reporter Occupation | RISK MANAGER |
| 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 | WECK |
| Generic Name | CURRETTE #2 |
| Product Code | HHK |
| Date Received | 2013-03-12 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PILLING WECK |
| Manufacturer Address | 4024 STIRRUP CREEK RESEARCH TRIANGLE PARK NC 27703 US 27703 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization | 2013-03-12 |