MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-15 for ELECTRICAL UMBILICAL CABLE 2035UC manufactured by Medtronic Cryocath Lp.
[136595969]
If information is provided in the future, a supplemental report will be issued.
Patient Sequence No: 1, Text Type: N, H10
[136595970]
It was reported that prior to a cryo ablation procedure, the packaging of six electrical umbilical cables were easier to open than normal and the sterility of the cables was questioned. There was no patient involvement.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3002648230-2019-00089 |
| MDR Report Key | 8342598 |
| Date Received | 2019-02-15 |
| Date of Report | 2019-03-15 |
| Date of Event | 2019-01-18 |
| Date Mfgr Received | 2019-02-19 |
| Device Manufacturer Date | 2018-09-27 |
| Date Added to Maude | 2019-02-15 |
| 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 | LISA ROBERTSON |
| Manufacturer Street | 8200 CORAL SEA ST NE |
| Manufacturer City | MOUNDS VIEW MN 55112 |
| Manufacturer Country | US |
| Manufacturer Postal | 55112 |
| Manufacturer Phone | 7635262723 |
| Manufacturer G1 | MEDTRONIC CRYOCATH LP |
| Manufacturer Street | 9000 AUTOROUTE TRANSCANADIENNE |
| Manufacturer City | POINTE-CLAIRE,QC H9R 5Z8 |
| Manufacturer Country | CA |
| Manufacturer Postal Code | H9R 5Z8 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | ELECTRICAL UMBILICAL CABLE |
| Generic Name | CABLE |
| Product Code | ISN |
| Date Received | 2019-02-15 |
| Returned To Mfg | 2019-02-01 |
| Model Number | 2035UC |
| Catalog Number | 2035UC |
| Lot Number | 33809 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MEDTRONIC CRYOCATH LP |
| Manufacturer Address | 9000 AUTOROUTE TRANSCANADIENNE POINTE-CLAIRE,QC H9R 5Z8 CA H9R 5Z8 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-02-15 |