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 2017-10-02 for UNKNOWN SUTURE manufactured by Ethicon Inc..
[88073263]
Attempts have been made to retrieve the device. To date the device has not been returned. If the device or further details are received at the later date a supplemental medwatch will be sent. Attempts are being made to obtain the additional information. To date no response has been provided. If further details are received at the later date a supplemental medwatch will be sent. Please provide the product code and the lot number of the product used, as already stated no further information is available.
Patient Sequence No: 1, Text Type: N, H10
[88073264]
It was reported that a rodent underwent a test procedure on (b)(6) 2017 and the unknown suture was used. It was also reported that the unknown suture/wire easily broke. Additional information has been requested.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2210968-2017-70388 |
MDR Report Key | 6909188 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2017-10-02 |
Date of Report | 2017-09-04 |
Date of Event | 2017-09-04 |
Date Mfgr Received | 2017-09-04 |
Date Added to Maude | 2017-10-02 |
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 | DARLENE KYLE |
Manufacturer Street | P.O. BOX 151, ROUTE 22 WEST |
Manufacturer City | SOMERVILLE 088760151 |
Manufacturer Country | US |
Manufacturer Postal | 088760151 |
Manufacturer Phone | 9082182792 |
Manufacturer G1 | ETHICON INC. |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNKNOWN SUTURE |
Generic Name | SUTURE, NONABSORBABLE |
Product Code | GAO |
Date Received | 2017-10-02 |
Catalog Number | UNK |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ETHICON INC. |
Manufacturer Address | P.O. BOX 151, ROUTE 22 WEST SOMERVILLE 088760151 US 088760151 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-10-02 |