MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-07 for INFANT CPR BAG 1056153 manufactured by Mercury Enterprises, Inc..
Report Number | 9161155 |
MDR Report Key | 9161155 |
Date Received | 2019-10-07 |
Date of Report | 2019-09-27 |
Date of Event | 2019-06-10 |
Report Date | 2019-09-27 |
Date Reported to FDA | 2019-09-27 |
Date Reported to Mfgr | 2019-10-07 |
Date Added to Maude | 2019-10-07 |
Event Key | 0 |
Report Source Code | User Facility 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 | INFANT CPR BAG |
Generic Name | VENTILATOR, EMERGENCY, MANUAL (RESUSCITATOR) |
Product Code | BTM |
Date Received | 2019-10-07 |
Catalog Number | 1056153 |
Lot Number | 1815856153 |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MERCURY ENTERPRISES, INC. |
Manufacturer Address | 11300 49TH ST. NORTH CLEARWATER FL 33762 US 33762 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-10-07 |