MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-26 for OUS PI PICC KIT: 2-L 5.5FR X 50CM CG+ IPN037551 CDA-45052-HPK1A manufactured by Arrow International Inc..
[185111923]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[185111924]
It was reported that lumen is occluded. The device was not removed. The team is using ucarinase in an attempt to unblock the picc rather than remove the device.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1036844-2020-00127 |
| MDR Report Key | 9885420 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2020-03-26 |
| Date of Report | 2020-03-13 |
| Date of Event | 2020-03-01 |
| Date Mfgr Received | 2020-03-13 |
| Device Manufacturer Date | 2019-07-02 |
| Date Added to Maude | 2020-03-26 |
| 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 | MARGIE BURTON, RN |
| Manufacturer Street | 3015 CARRINGTON MILL BLVD |
| Manufacturer City | MORRISVILLE NC 27560 |
| Manufacturer Country | US |
| Manufacturer Postal | 27560 |
| Manufacturer Phone | 9194334965 |
| Manufacturer G1 | ARROW INTERNATIONAL INC. |
| Manufacturer Street | 312 COMMERCE PLACE |
| Manufacturer City | ASHEBORO NC 27203 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 27203 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | OUS PI PICC KIT: 2-L 5.5FR X 50CM CG+ |
| Generic Name | CATHETER,INTRAVASCULAR,THERAP |
| Product Code | LJS |
| Date Received | 2020-03-26 |
| Model Number | IPN037551 |
| Catalog Number | CDA-45052-HPK1A |
| Lot Number | 23F19G0074 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | ARROW INTERNATIONAL INC. |
| Manufacturer Address | READING PA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2020-03-26 |