MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-01 for AOSEPT PLUS/CLEAR CARE CLEANING AND DISINFECTING SOLUTION 0065035821 manufactured by Alcon Research, Llc.
Report Number | 1610287-2019-00027 |
MDR Report Key | 9142691 |
Date Received | 2019-10-01 |
Date of Report | 2019-12-02 |
Date of Event | 2019-09-01 |
Date Mfgr Received | 2019-11-15 |
Device Manufacturer Date | 2019-03-25 |
Date Added to Maude | 2019-10-01 |
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. CINDY MILAM |
Manufacturer Street | 6201 SOUTH FREEWAY MAIL STOP AB2-6 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8176152231 |
Manufacturer G1 | ALCON RESEARCH, LLC |
Manufacturer Street | 6201 SOUTH FREEWAY |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal Code | 76134 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AOSEPT PLUS/CLEAR CARE CLEANING AND DISINFECTING SOLUTION |
Generic Name | ACCESSORIES, SOFT LENS PRODUCTS |
Product Code | LPN |
Date Received | 2019-10-01 |
Model Number | NA |
Catalog Number | 0065035821 |
Lot Number | 305917F |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ALCON RESEARCH, LLC |
Manufacturer Address | 6201 SOUTH FREEWAY FORT WORTH TX 76134 US 76134 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-10-01 |