MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-20 for LIFEPORT KIDNEY TRANSPORTER SYSTEM LKT200 manufactured by Organ Recovery Systems, Inc..
Report Number | 3004068499-2020-00005 |
MDR Report Key | 9862315 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2020-03-20 |
Date of Report | 2020-03-20 |
Date of Event | 2020-02-21 |
Date Mfgr Received | 2020-02-21 |
Device Manufacturer Date | 2019-10-29 |
Date Added to Maude | 2020-03-20 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MS. ROXANNE GEARY |
Manufacturer Street | 1 PIERCE PLACE SUITE 475W |
Manufacturer City | ITASCA, IL |
Manufacturer Country | US |
Manufacturer Phone | 8242600 |
Manufacturer G1 | ORGAN RECOVERY SYSTEMS, INC. |
Manufacturer Street | 1 PIERCE PLACE SUITE 475W |
Manufacturer City | ITASCA, IL |
Manufacturer Country | US |
Single Use | 3 |
Remedial Action | RL |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LIFEPORT KIDNEY TRANSPORTER SYSTEM |
Generic Name | PERFUSION CIRCUIT |
Product Code | KDN |
Date Received | 2020-03-20 |
Returned To Mfg | 2020-03-03 |
Model Number | LKT200 |
Catalog Number | LKT200 |
Lot Number | 121821 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ORGAN RECOVERY SYSTEMS, INC. |
Manufacturer Address | 1 PIERCE PLACE SUITE 475W ITASCA, IL US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-20 |