MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-10-17 for DERMATOUCH LP SMALL LATEX GLOVE manufactured by Unknown.
[57977803]
My cat required emergency medical care and was transferred from my local vet to (b)(6) clinic. I told them that i had a severe latex allergy but they did not remove latex products from the area and continued to use latex gloves and possible a catheter on my cat throughout his 8 day stay and post-op visit. I've experienced hives, wheezing, asthma attacks and diarrhea during my cat's care.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5065489 |
| MDR Report Key | 6039515 |
| Date Received | 2016-10-17 |
| Date of Report | 2016-10-17 |
| Date of Event | 2016-09-30 |
| Date Added to Maude | 2016-10-19 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 0 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | DERMATOUCH LP SMALL LATEX GLOVE |
| Generic Name | DERMATOUCH LP SMALL LATEX GLOVE |
| Product Code | LYY |
| Date Received | 2016-10-17 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | UNKNOWN |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Deathisabilit | 2016-10-17 |