MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-08 for GELCLAIR manufactured by Midatech / Helsinn Healthcare Sa.
[174660297]
Pt stated that after using gelclair a couple of times, she experienced a burning sensation in her mouth. Pt states that she followed directions for usage exactly as indicated and prescribed.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5092116 |
| MDR Report Key | 9569389 |
| Date Received | 2020-01-08 |
| Date of Report | 2020-01-06 |
| Date of Event | 2020-01-02 |
| Date Added to Maude | 2020-01-09 |
| 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 |
| Reporter Occupation | PHARMACIST |
| 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 | GELCLAIR |
| Generic Name | DRESSING, WOUND, DRUG |
| Product Code | FRO |
| Date Received | 2020-01-08 |
| Lot Number | 078811 |
| Device Availability | N |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MIDATECH / HELSINN HEALTHCARE SA |
| Product Code | --- |
| Date Received | 2020-01-08 |
| Device Sequence No | 101 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-01-08 |