MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2014-10-21 for LATEX GLOVES manufactured by .
[5041379]
He is suffering from hypoglycemia and allergic reaction to latex gloves since 1985. Without taking proper medication for hypoglycemia, he could have severe shaking, sweating anxiety, dizziness, fatigue and impaired vision. I recommend that he use powder less gloves to avoid rashes on hands and face.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5038793 |
| MDR Report Key | 4199278 |
| Date Received | 2014-10-21 |
| Date of Report | 2014-10-21 |
| Date of Event | 1985-01-01 |
| Date Added to Maude | 2014-10-27 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | LATEX GLOVES |
| Generic Name | LATEX GLOVES |
| Product Code | LYY |
| Date Received | 2014-10-21 |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2014-10-21 |