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 2020-03-30 for ENDO STITCH 173016 manufactured by Davis & Geck Caribe Ltd.
[186148148]
(b)(4). If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[186148149]
According to the reporter, during a total laparoscopic hysterectomy, prior to the end of the case, it was noticed that a piece of the needle was missing. The device component fell into the cavity of the patient. A cystoscopy was done and the needle was found in the bladder that was removed with a laparoscopic grasper.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9612501-2020-00553 |
MDR Report Key | 9901670 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-30 |
Date of Report | 2020-03-30 |
Date Mfgr Received | 2020-03-11 |
Device Manufacturer Date | 2019-10-09 |
Date Added to Maude | 2020-03-30 |
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 | LISA HERNANDEZ |
Manufacturer Street | 60 MIDDLETOWN AVE. |
Manufacturer City | NORTH HAVEN CT 06473 |
Manufacturer Country | US |
Manufacturer Postal | 06473 |
Manufacturer Phone | 2034925563 |
Manufacturer G1 | DAVIS & GECK CARIBE LTD |
Manufacturer Street | ZONA FRANCA DE SAN ISIDRO |
Manufacturer City | SANTO DOMINGO 0101 |
Manufacturer Country | DO |
Manufacturer Postal Code | 0101 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ENDO STITCH |
Generic Name | ENDOSCOPIC TISSUE APPROXIMATION DEVICE |
Product Code | OCW |
Date Received | 2020-03-30 |
Model Number | 173016 |
Catalog Number | 173016 |
Lot Number | J9K1074EY |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | DAVIS & GECK CARIBE LTD |
Manufacturer Address | ZONA FRANCA DE SAN ISIDRO SANTO DOMINGO 0101 DO 0101 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-30 |