MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2020-03-11 for BARD? X-FORCE? BALLOON DILATION CATHETER 998806 manufactured by C.r. Bard, Inc. (covington) -1018233.
[186414050]
The investigation is still in progress. Once the investigation is complete, a supplemental report will be filed. The device was not returned.
Patient Sequence No: 1, Text Type: N, H10
[186414051]
It was reported that fluid leaked from the stopcock connector. The event occurred while fluids were being injected into the balloon using the eagle inflation device during ureterostenosis expansion procedure. The stopcock was confirmed to be firmly in place.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1018233-2020-01753 |
MDR Report Key | 9820381 |
Report Source | COMPANY REPRESENTATIVE,OTHER |
Date Received | 2020-03-11 |
Date of Report | 2020-03-11 |
Date of Event | 2020-01-14 |
Date Mfgr Received | 2020-02-19 |
Date Added to Maude | 2020-03-11 |
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 | YONIC ANDERSON |
Manufacturer Street | 8195 INDUSTRIAL BLVD |
Manufacturer City | COVINGTON GA 30014 |
Manufacturer Country | US |
Manufacturer Postal | 30014 |
Manufacturer Phone | 7707846100 |
Manufacturer G1 | C.R. BARD, INC. (COVINGTON) -1018233 |
Manufacturer Street | 8195 INDUSTRIAL BLVD |
Manufacturer City | COVINGTON GA 30014 |
Manufacturer Country | US |
Manufacturer Postal Code | 30014 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BARD? X-FORCE? BALLOON DILATION CATHETER |
Generic Name | X-FORCE URETERAL DILATION BALLOON CATHETER KIT |
Product Code | EZN |
Date Received | 2020-03-11 |
Model Number | 998806 |
Catalog Number | 998806 |
Lot Number | BMCUFM39 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | C.R. BARD, INC. (COVINGTON) -1018233 |
Manufacturer Address | 8195 INDUSTRIAL BLVD COVINGTON GA 30014 US 30014 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-11 |