MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-16 for MEPILEX DRESSING BORDER POST-OP AG 498600 manufactured by Molynlycke Healthcare Us Llc.
[175852486]
Mepilex border post-op ag dressing noticed to be discolored when introduced to the surgical field. Fda safety report id# (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5092322 |
| MDR Report Key | 9601403 |
| Date Received | 2020-01-16 |
| Date of Report | 2020-01-15 |
| Date of Event | 2020-01-14 |
| Date Added to Maude | 2020-01-17 |
| 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 |
| 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 | 3 |
| Brand Name | MEPILEX DRESSING BORDER POST-OP AG |
| Generic Name | DRESSING, WOUND DRUG |
| Product Code | FRO |
| Date Received | 2020-01-16 |
| Model Number | 498600 |
| Catalog Number | 498600 |
| Lot Number | 19187779 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MOLYNLYCKE HEALTHCARE US LLC |
| Manufacturer Address | NORCROSS GA 30092 US 30092 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-01-16 |