MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2020-03-04 for ARROW THORACENTESIS KIT AK-01000 manufactured by Arrow International Inc..
[184918839]
(b)(4).
Patient Sequence No: 1, Text Type: N, H10
[184918840]
The customer reports that when opening the thoracentesis kit with the more flimsy bottom, it was noted that the bottle of lidocaine was broken.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1036844-2020-00090 |
MDR Report Key | 9786207 |
Report Source | COMPANY REPRESENTATIVE,USER F |
Date Received | 2020-03-04 |
Date of Report | 2020-02-25 |
Date of Event | 2020-02-24 |
Date Mfgr Received | 2020-02-25 |
Date Added to Maude | 2020-03-04 |
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 | 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 | ARROW THORACENTESIS KIT |
Generic Name | CATHETER AND TIP SUCTION |
Product Code | JOL |
Date Received | 2020-03-04 |
Catalog Number | AK-01000 |
Lot Number | UNKNOWN |
Device Availability | N |
Device Age | DA |
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 | 2020-03-04 |