MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2017-02-24 for PREPEX manufactured by Circ Medtech.
[68209640]
No manufacturer investigation was undertaken since this was a foreseen risk in device usage and is clearly noted both in the ifu and the training program.
Patient Sequence No: 1, Text Type: N, H10
[68209641]
Patient attempted to self remove device leading to edema and was referred to surgical circumcision.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3011215095-2017-00920 |
MDR Report Key | 6355952 |
Report Source | USER FACILITY |
Date Received | 2017-02-24 |
Date of Report | 2017-02-24 |
Date of Event | 2016-10-21 |
Date Mfgr Received | 2017-02-10 |
Date Added to Maude | 2017-02-24 |
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 | 0 |
Initial Report to FDA | 0 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS OSSIE MILANOV |
Manufacturer Street | 1 HANAGAR ST. |
Manufacturer City | HOD HASHARON, 4501305 |
Manufacturer Country | IS |
Manufacturer Postal | 4501305 |
Manufacturer Phone | 97994949 |
Manufacturer G1 | 3BY |
Manufacturer Street | TEFEN INDUSTRIAL ZONE |
Manufacturer City | TEFEN, 24959 |
Manufacturer Country | IS |
Manufacturer Postal Code | 24959 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PREPEX |
Generic Name | PREPEX |
Product Code | HFX |
Date Received | 2017-02-24 |
Operator | NURSE |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CIRC MEDTECH |
Manufacturer Address | 1 HANAGAR ST. HOD HASHARON, 4501305 IS 4501305 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2017-02-24 |