MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-22 for LOVE-GRUENWALD PITUITARY FORCEPS 2X10MM NL6146 manufactured by Carefusion, Inc.
Report Number | 1423507-2019-00011 |
MDR Report Key | 8811440 |
Date Received | 2019-07-22 |
Date of Report | 2019-07-22 |
Date of Event | 2019-06-18 |
Date Mfgr Received | 2019-06-18 |
Device Manufacturer Date | 2017-10-01 |
Date Added to Maude | 2019-07-22 |
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 | BDX ANNA WEHRHEIM |
Manufacturer Street | 75 NORTH FAIRWAY DRIVE |
Manufacturer City | VERNON HILLS IL 60061 |
Manufacturer Country | US |
Manufacturer Postal | 60061 |
Manufacturer Phone | 8015652341 |
Manufacturer G1 | CAREFUSION, INC |
Manufacturer Street | 75 NORTH FAIRWAY DRIVE |
Manufacturer City | VERNON HILLS IL 60061 |
Manufacturer Country | US |
Manufacturer Postal Code | 60061 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | LOVE-GRUENWALD PITUITARY FORCEPS 2X10MM |
Generic Name | KERRISON RONGEURS |
Product Code | HAE |
Date Received | 2019-07-22 |
Catalog Number | NL6146 |
Lot Number | J17XSX |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CAREFUSION, INC |
Manufacturer Address | 75 NORTH FAIRWAY DRIVE VERNON HILLS IL 60061 US 60061 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-07-22 |