MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,health pr report with the FDA on 2018-12-06 for ARROW HEMODIALYSIS SET: 2-LUMEN 12 FR X 20 CM CS-15122-F manufactured by Arrow International Inc..
        [129478800]
Qn# (b)(4).
 Patient Sequence No: 1, Text Type: N, H10
        [129478801]
Complaint description: though resistance was met when advancing guidewire through ars, the physician still managed to make it through. However, he/she couldn't advance it further when guidewire tip reached blood vessel. Guidewire was removed and found it kinked.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3006425876-2018-00761 | 
| MDR Report Key | 8137686 | 
| Report Source | DISTRIBUTOR,FOREIGN,HEALTH PR | 
| Date Received | 2018-12-06 | 
| Date of Report | 2018-11-21 | 
| Date of Event | 2018-11-16 | 
| Date Mfgr Received | 2019-01-10 | 
| Device Manufacturer Date | 2018-02-28 | 
| Date Added to Maude | 2018-12-06 | 
| 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 | KATHARINE TARPLEY | 
| Manufacturer Street | 3015 CARRINGTON MILL BLVD | 
| Manufacturer City | MORRISVILLE NC 27560 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 27560 | 
| Manufacturer Phone | 9194334854 | 
| Manufacturer G1 | ARROW INTERNATIONAL CR, A.S. | 
| Manufacturer Street | JAMSKA 2359/47 | 
| Manufacturer City | ZDAR NAD SAZAVOU 591 01 | 
| Manufacturer Country | EZ | 
| Manufacturer Postal Code | 591 01 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | ARROW HEMODIALYSIS SET: 2-LUMEN 12 FR X 20 CM | 
| Generic Name | CATHETER SUBCLAVIAN | 
| Product Code | LFJ | 
| Date Received | 2018-12-06 | 
| Returned To Mfg | 2018-11-27 | 
| Catalog Number | CS-15122-F | 
| Lot Number | 71F18B3092 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | R | 
| Device Age | DA | 
| Device Eval'ed by Mfgr | Y | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | ARROW INTERNATIONAL INC. | 
| Manufacturer Address | READING PA | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2018-12-06 |