MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-03-30 for CARDINAL HEALTH COVIDIEN 2841 manufactured by Covidien.
[72175009]
We contacted multicare (b)(4), they pulled 2 boxes and have contacted the vendor to return the 2 boxes. They will send me a return label and i will send them back to vendor.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5068894 |
| MDR Report Key | 6459779 |
| Date Received | 2017-03-30 |
| Date Added to Maude | 2017-04-05 |
| 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 | OTHER HEALTH CARE PROFESSIONAL |
| 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 | CARDINAL HEALTH COVIDIEN |
| Generic Name | CURITY EYE PAD |
| Product Code | HMP |
| Date Received | 2017-03-30 |
| Model Number | 2841 |
| Lot Number | 15M000000 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN |
| Brand Name | CARDINAL HEALTH COVIDIEN |
| Generic Name | CURITY EYE PAD |
| Product Code | HMP |
| Date Received | 2017-03-30 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 2 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2017-03-30 |