MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2014-01-06 for HEPARIN FLUSHING NEEDLE 310383 manufactured by Integra York, Pa Inc..
[15125248]
Customer initially reports needle broke during a procedure. No patient injury. On (b)(6)2013, customer reports doctor was performing a carotid endarterectomy. Device snapped in 2 pieces at the connection of the hub and the needle. No x-ray because they had all the parts.
Patient Sequence No: 1, Text Type: D, B5
[15465997]
The device involved in the reported incident has been received for evaluation. An investigation has been initiated based on the reported information.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2523190-2013-00076 |
| MDR Report Key | 3695346 |
| Report Source | 06 |
| Date Received | 2014-01-06 |
| Date of Report | 2013-12-11 |
| Date of Event | 2013-12-11 |
| Date Mfgr Received | 2013-12-23 |
| Date Added to Maude | 2014-04-17 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| 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 |
| Manufacturer Contact | SANDRA LEE |
| Manufacturer Street | 315 ENTERPRISE DR |
| Manufacturer Phone | 6099366828 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HEPARIN FLUSHING NEEDLE |
| Generic Name | CARDIOVASCULAR GENERAL |
| Product Code | GDM |
| Date Received | 2014-01-06 |
| Catalog Number | 310383 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | INTEGRA YORK, PA INC. |
| Manufacturer Address | YORK PA 17402 US 17402 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2014-01-06 |