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 2019-11-20 for LIFEPORT KIDNEY TRANSPORTER SYSTEM LKT200 manufactured by Organ Recovery Systems, Inc..
Report Number | 3004068499-2019-00002 |
MDR Report Key | 9349319 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2019-11-20 |
Date of Report | 2019-11-20 |
Date of Event | 2019-10-20 |
Date Mfgr Received | 2019-10-23 |
Device Manufacturer Date | 2019-06-17 |
Date Added to Maude | 2019-11-20 |
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 60143 |
Manufacturer Country | US |
Manufacturer Postal | 60143 |
Manufacturer Phone | 8478242436 |
Manufacturer G1 | ORGAN RECOVERY SYSTEMS, INC. |
Manufacturer Street | 1 PIERCE PLACE SUITE 475W |
Manufacturer City | ITASCA IL 60143 |
Manufacturer Country | US |
Manufacturer Postal Code | 60143 |
Single Use | 3 |
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 | 2019-11-20 |
Returned To Mfg | 2019-11-08 |
Model Number | LKT200 |
Catalog Number | LKT200 |
Lot Number | 76657831 |
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 60143 US 60143 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-20 |