MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-08 for TELFA AMD ANTIMICROBIAL NON-ADHERENT PAD manufactured by Covidien / Cardinal Health 200 Llc.
[141454843]
Covidien telfa amd antimicrobial non-adherent pad 3" x 8" ref 7663.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5085675 |
| MDR Report Key | 8496701 |
| Date Received | 2019-04-08 |
| Date of Report | 2019-03-28 |
| Date of Event | 2019-03-26 |
| Date Added to Maude | 2019-04-09 |
| 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 | RISK MANAGER |
| 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 | TELFA AMD ANTIMICROBIAL NON-ADHERENT PAD |
| Generic Name | GAUZE, SPONGE, INTERNAL |
| Product Code | EFQ |
| Date Received | 2019-04-08 |
| Lot Number | 19A154962 |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN / CARDINAL HEALTH 200 LLC |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-04-08 |