MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional report with the FDA on 2019-08-16 for CAPTURA SERRATED FORCEPS W/O SPIKE G56126 DBF-2.4SN-230-20-S manufactured by Cook Endoscopy.
Report Number | 1037905-2019-00468 |
MDR Report Key | 8903236 |
Report Source | FOREIGN,HEALTH PROFESSIONAL |
Date Received | 2019-08-16 |
Date of Report | 2019-07-08 |
Date of Event | 2019-07-05 |
Date Mfgr Received | 2019-07-23 |
Device Manufacturer Date | 2019-01-29 |
Date Added to Maude | 2019-08-16 |
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 | 3 |
Event Location | 3 |
Manufacturer Contact | MS. SCOTTIE FARIOLE |
Manufacturer Street | 4900 BETHANIA STATION RD |
Manufacturer City | WINSTON-SALEM NC 27105 |
Manufacturer Country | US |
Manufacturer Postal | 27105 |
Manufacturer Phone | 3367440157 |
Manufacturer G1 | COOK ENDOSCOPY |
Manufacturer Street | 4900 BETHANIA STATION RD |
Manufacturer City | WINSTON-SALEM NC 27105 |
Manufacturer Country | US |
Manufacturer Postal Code | 27105 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CAPTURA SERRATED FORCEPS W/O SPIKE |
Generic Name | PTS ENDOSCOPIC GRASPING/CUTTING INSTRUMENT, NON-POWERED, EXEMPT |
Product Code | PTS |
Date Received | 2019-08-16 |
Returned To Mfg | 2019-07-23 |
Model Number | G56126 |
Catalog Number | DBF-2.4SN-230-20-S |
Lot Number | W4170933 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOK ENDOSCOPY |
Manufacturer Address | 4900 BETHANIA STATION RD WINSTON-SALEM NC 27105 US 27105 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-16 |