MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-02-19 for PNEUPAC PARAPAC PLUS 310 P310NUS manufactured by Smiths Medical Asd; Inc..
[180113073]
Information was received indicating that an internal leak occurred to a smiths medical pneupac parapac plus. There were no reported adverse effects.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3012307300-2020-01160 |
MDR Report Key | 9730084 |
Report Source | USER FACILITY |
Date Received | 2020-02-19 |
Date of Report | 2020-03-25 |
Date Mfgr Received | 2020-02-24 |
Device Manufacturer Date | 2007-08-31 |
Date Added to Maude | 2020-02-19 |
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 Contact | DAVE HALVERSON |
Manufacturer Street | 6000 NATHAN LANE N |
Manufacturer City | MINNEAPOLIS, MN 55442 |
Manufacturer Country | US |
Manufacturer Postal | 55442 |
Manufacturer Phone | 7633833310 |
Manufacturer G1 | SMITHS MEDICAL ASD; INC. |
Manufacturer Street | 6000 NATHAN LANE N |
Manufacturer City | MINNEAPOLIS, MN 55442 |
Manufacturer Country | US |
Manufacturer Postal Code | 55442 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PNEUPAC PARAPAC PLUS |
Generic Name | VENTILATOR, EMERGENCY, POWERED (RESUSCITATOR) |
Product Code | BTL |
Date Received | 2020-02-19 |
Returned To Mfg | 2020-01-27 |
Model Number | 310 |
Catalog Number | P310NUS |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITHS MEDICAL ASD; INC. |
Manufacturer Address | 6000 NATHAN LANE N MINNEAPOLIS, MN 55442 US 55442 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-02-19 |