MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-22 for ACUVUE OASYS DISPOSABLE SOFT CONTACT LENS manufactured by Johnson & Johnson Vision Care, Inc..
Report Number | MW5090575 |
MDR Report Key | 9225135 |
Date Received | 2019-10-22 |
Date of Report | 2019-10-19 |
Date of Event | 2019-10-19 |
Date Added to Maude | 2019-10-23 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
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 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | ACUVUE OASYS DISPOSABLE SOFT CONTACT LENS |
Generic Name | LENS, CONTACT, (DISPOSABLE) |
Product Code | MVN |
Date Received | 2019-10-22 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | JOHNSON & JOHNSON VISION CARE, INC. |
Manufacturer Address | JACKSONVILLE FL 32256 US 32256 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-10-22 |