MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-04 for 8.5MM/2.8MM WIRE SLEEVE 312.08 manufactured by Wrights Lane Synthes Usa Products Llc.
Report Number | 2939274-2019-61211 |
MDR Report Key | 9158396 |
Date Received | 2019-10-04 |
Date of Report | 2019-08-15 |
Date Mfgr Received | 2019-09-16 |
Device Manufacturer Date | 2009-03-26 |
Date Added to Maude | 2019-10-04 |
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 |
Manufacturer G1 | WERK H |
Manufacturer Street | IM BIFANG 6 |
Manufacturer City | HAEGENDORF 4614 |
Manufacturer Country | SZ |
Manufacturer Postal Code | 4614 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | 8.5MM/2.8MM WIRE SLEEVE |
Generic Name | MISC ORTHO SURGICAL INSTR |
Product Code | LHX |
Date Received | 2019-10-04 |
Returned To Mfg | 2019-08-29 |
Model Number | 312.08 |
Catalog Number | 312.08 |
Lot Number | 3121840 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
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 | 2019-10-04 |