MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2004-04-08 for WALGREENS ONE STEP DISINFECTING-SOLUTION * manufactured by Sauflon Pharmaceuticals, Ltd..
[22184770]
Pt's eyes got irritated after using the solution they thought they had bought an eye disinfectant solution. Alleged that medical assistance was sought and a patch was placed on their right eye.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2438562-2004-00012 |
| MDR Report Key | 521198 |
| Date Received | 2004-04-08 |
| Date of Report | 2004-02-09 |
| Date of Event | 2003-10-10 |
| Date Facility Aware | 2004-02-09 |
| Report Date | 2004-02-09 |
| Date Reported to Mfgr | 2004-02-09 |
| Date Added to Maude | 2004-04-21 |
| Event Key | 0 |
| Report Source Code | Distributor report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | WALGREENS ONE STEP DISINFECTING-SOLUTION |
| Generic Name | HYDROGEN PEROXIDE LENS CARE SYSTEM |
| Product Code | MRC |
| Date Received | 2004-04-08 |
| Model Number | * |
| Catalog Number | * |
| Lot Number | UNK |
| ID Number | * |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Age | UNKNOWN |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 510306 |
| Manufacturer | SAUFLON PHARMACEUTICALS, LTD. |
| Manufacturer Address | * TWICKENHAM, MIDDLESEX UK |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2004-04-08 |