MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2010-06-16 for PILLING ASPIRATING NEEDLE 23GA * 507454 manufactured by Teleflex Medical.
[14965379]
Mediastinoscopy aspirating needle tip noted to be broken off when removed from patient's chest. Area searched, chest x-ray done. Total tip found when checking suction manifold.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1728726 |
| MDR Report Key | 1728726 |
| Date Received | 2010-06-16 |
| Date of Report | 2010-06-16 |
| Date of Event | 2010-06-01 |
| Report Date | 2010-06-16 |
| Date Reported to FDA | 2010-06-16 |
| Date Added to Maude | 2010-06-18 |
| 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 | 0 |
| 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 | PILLING ASPIRATING NEEDLE 23GA |
| Generic Name | ASPIRATING NEEDLE |
| Product Code | GAI |
| Date Received | 2010-06-16 |
| Model Number | * |
| Catalog Number | 507454 |
| Lot Number | UU7 (LOT # FROM A NEW PKG) |
| ID Number | * |
| Operator | PHYSICIAN |
| Device Availability | Y |
| Device Age | 1 DY |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | TELEFLEX MEDICAL |
| Manufacturer Address | 4024 STIRRUP CREEK DR. SUITE 720 DURHAM NC 27703 US 27703 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2010-06-16 |