MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2019-08-29 for PROPAQ MD DEFIBRILLATOR manufactured by Zoll Medical Corporation.
| Report Number | 1220908-2019-02563 |
| MDR Report Key | 8946035 |
| Report Source | FOREIGN |
| Date Received | 2019-08-29 |
| Date of Report | 2019-08-10 |
| Date Mfgr Received | 2019-08-10 |
| Device Manufacturer Date | 2017-11-01 |
| Date Added to Maude | 2019-08-29 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| 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 |
| Manufacturer Street | 269 MILL ROAD |
| Manufacturer City | CHELMSFORD MA 01824 |
| Manufacturer Country | US |
| Manufacturer Postal | 01824 |
| Manufacturer Phone | 9784219552 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PROPAQ MD DEFIBRILLATOR |
| Generic Name | PROPAQ MD |
| Product Code | DRO |
| Date Received | 2019-08-29 |
| Returned To Mfg | 2019-08-28 |
| Model Number | PROPAQ MD |
| Catalog Number | PROPAQ MD |
| Lot Number | NA |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Manufacturer Address | 269 MILL ROAD CHELMSFORD MA 01824 US 01824 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-08-29 |