MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-08-26 for UNK - CABLE/WIRE: TRAUMA manufactured by Wrights Lane Synthes Usa Products Llc.
Report Number | 2939274-2019-60105 |
MDR Report Key | 8932780 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-08-26 |
Date of Report | 2019-07-29 |
Date Mfgr Received | 2019-10-01 |
Date Added to Maude | 2019-08-26 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | KARA DITTY-BOVARD |
Manufacturer Street | 1302 WRIGHTS LANE EAST |
Manufacturer City | WEST CHESTER PA 19380 |
Manufacturer Country | US |
Manufacturer Postal | 19380 |
Manufacturer Phone | 6103142063 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNK - CABLE/WIRE: TRAUMA |
Generic Name | WIRE,SURGICAL TRAY, SUGRICAL |
Product Code | LRN |
Date Received | 2019-08-26 |
Returned To Mfg | 2019-10-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | WRIGHTS LANE SYNTHES USA PRODUCTS LLC |
Manufacturer Address | 1302 WRIGHTS LANE EAST WEST CHESTER PA 19380 US 19380 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-26 |