MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-03-17 for BIOFINITY TORIC (COMFILCON A) manufactured by Coopervision Manufacturing, Ltd..
Report Number | 9614392-2020-00005 |
MDR Report Key | 9842297 |
Report Source | CONSUMER |
Date Received | 2020-03-17 |
Date of Report | 2020-03-17 |
Date Mfgr Received | 2020-02-16 |
Device Manufacturer Date | 2019-09-18 |
Date Added to Maude | 2020-03-17 |
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 | MS. MELISSA TORPEY |
Manufacturer Street | 5870 STONERIDGE DRIVE SUITE 1 |
Manufacturer City | PLEASANTON, CA |
Manufacturer Country | US |
Manufacturer Phone | 7569874 |
Manufacturer G1 | COOPERVISION MANUFACTURING, LTD. |
Manufacturer Street | SOUTH POINT HAMBLE UNIT 2 |
Manufacturer City | SOUTHAMPTOM, HAMPSHIRE SO314RF |
Manufacturer Country | UK |
Manufacturer Postal Code | SO31 4RF |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BIOFINITY TORIC (COMFILCON A) |
Generic Name | BIOFINITY TORIC (COMFILCON A) |
Product Code | LPM |
Date Received | 2020-03-17 |
Returned To Mfg | 2020-03-01 |
Lot Number | 12607000047006 |
Operator | LAY USER/PATIENT |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOPERVISION MANUFACTURING, LTD. |
Manufacturer Address | SOUTH POINT HAMBLE UNIT 2 SOUTHAMPTOM, HAMPSHIRE SO314RF UK SO31 4RF |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-17 |