MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2019-11-14 for ACUVUE? OASYS? FOR PRESBYOPIA ALP manufactured by Johnson & Johnson Vision Care, Inc. ? Us.
| Report Number | 1057985-2019-00121 |
| MDR Report Key | 9323160 |
| Report Source | OTHER |
| Date Received | 2019-11-14 |
| Date of Report | 2019-10-21 |
| Date of Event | 2018-12-10 |
| Date Mfgr Received | 2019-10-21 |
| Device Manufacturer Date | 2018-07-25 |
| Date Added to Maude | 2019-11-14 |
| 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 | ROSE HARRELL |
| Manufacturer Street | 7500 CENTURION PARKWAY |
| Manufacturer City | JACKSONVILLE FL 32256 |
| Manufacturer Country | US |
| Manufacturer Postal | 32256 |
| Manufacturer Phone | 9044433364 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | ACUVUE? OASYS? FOR PRESBYOPIA |
| Generic Name | LENSES, SOFT CONTACT, EXTENDED WEAR |
| Product Code | LPM |
| Date Received | 2019-11-14 |
| Model Number | NA |
| Catalog Number | ALP |
| Lot Number | B00QWN1 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | JOHNSON & JOHNSON VISION CARE, INC. ? US |
| Manufacturer Address | 7500 CENTURION PARKWAY JACKSONVILLE FL US |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other; 2. Required No Informationntervention; 3. Deathisabilit | 2019-11-14 |