MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-09-02 for NO BRAND NAME ON STETHOSCOPE NO # AVAILABLE manufactured by .
[1702573]
While removing stethoscope, the metal spring broke in half and left a 1 cm deep laceration on the anterior chest (1/2" long) of the medical assistant.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5017315 |
| MDR Report Key | 1828582 |
| Date Received | 2010-09-02 |
| Date of Report | 2010-09-01 |
| Date of Event | 2010-08-25 |
| Date Added to Maude | 2010-09-13 |
| 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 | NO BRAND NAME ON STETHOSCOPE |
| Generic Name | STETHOSCOPE |
| Product Code | LDE |
| Date Received | 2010-09-02 |
| Model Number | NO # AVAILABLE |
| Catalog Number | NA |
| Lot Number | NA |
| ID Number | NA |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2010-09-02 |