MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-30 for POLYSORB GLS-122 manufactured by Davis & Geck Caribe Ltd.
[185501037]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[185501038]
According to the reporter, during a laparoscopic procedure, the thread broke under very little tension. Another device from different lot number was used to complete the case. There was no patient injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 9612501-2020-00539 |
MDR Report Key | 9897296 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-30 |
Date of Report | 2020-03-30 |
Date of Event | 2020-03-06 |
Date Mfgr Received | 2020-03-11 |
Device Manufacturer Date | 2019-09-02 |
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 | POLYSORB |
Generic Name | SUTURE, ABSORBABLE, SYNTHETIC, POLYGLYCOLIC ACID |
Product Code | GAM |
Date Received | 2020-03-30 |
Model Number | GLS-122 |
Catalog Number | GLS-122 |
Lot Number | D9J0129Y |
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 | 2020-03-30 |