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 2020-02-14 for ENDO STITCH 173016 manufactured by Davis & Geck Caribe Ltd.
[179455246]
(b)(4). If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[179455247]
According to the reporter, during a total laparoscopic hysterectomy, while suturing the vaginal cuff, the needle broke and fell into the patient's cavity. An x-ray was performed to locate the needle but unable to retrieved. Surgical time was extended more than thirty minutes.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9612501-2020-00271 |
MDR Report Key | 9711965 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-02-14 |
Date of Report | 2020-02-14 |
Date of Event | 2019-09-23 |
Date Mfgr Received | 2020-01-31 |
Device Manufacturer Date | 2019-03-12 |
Date Added to Maude | 2020-02-14 |
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 | 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 | 2020-02-14 |
Model Number | 173016 |
Catalog Number | 173016 |
Lot Number | J9C1089EY |
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 | 2020-02-14 |