MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2015-03-19 for ARROW CONTINUOUS NERVE BLOCK KIT FB-19604-K manufactured by Arrow Intl., Inc..
[5590907]
The customer alleges that while using the flex block kit; the catheter kinked inside the needle. No patient injury or harm reported.
Patient Sequence No: 1, Text Type: D, B5
[13107853]
(b)(4). It is unknown if the device sample is available for evaluation.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1036844-2015-00073 |
MDR Report Key | 4620143 |
Report Source | 06,07 |
Date Received | 2015-03-19 |
Date of Report | 2015-02-20 |
Date of Event | 2015-02-20 |
Date Mfgr Received | 2015-02-20 |
Date Added to Maude | 2015-05-01 |
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 | 0 |
Event Location | 0 |
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 INTL., INC. |
Manufacturer Street | 312 COMMERCE PL. |
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 | ARROW CONTINUOUS NERVE BLOCK KIT |
Generic Name | ANESTHESIA CONDUCTION KIT |
Product Code | OGJ |
Date Received | 2015-03-19 |
Catalog Number | FB-19604-K |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ARROW INTL., INC. |
Manufacturer Address | READING PA US |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-03-19 |