MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-07-10 for DAVOL? INFANT CATH KIT 0035630 manufactured by C.r. Bard, Inc. (covington) -1018233.
[113910960]
The investigation is still in progress. Once the investigation is complete a supplemental report will be filed. The information provided by bard represents all of the known information at this time. Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bard. The device was not returned.
Patient Sequence No: 1, Text Type: N, H10
[113910961]
It was reported that urine did not drain when the pediatric catheter was inserted to collect a urine sample. However, when the catheter was removed, the patient released urine.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1018233-2018-02704 |
MDR Report Key | 7675512 |
Date Received | 2018-07-10 |
Date of Report | 2018-10-02 |
Date of Event | 2018-06-20 |
Date Mfgr Received | 2018-09-21 |
Device Manufacturer Date | 2017-02-17 |
Date Added to Maude | 2018-07-10 |
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 | 0 |
Brand Name | DAVOL? INFANT CATH KIT |
Generic Name | INFANT CATH KIT |
Product Code | FFH |
Date Received | 2018-07-10 |
Returned To Mfg | 2018-07-13 |
Catalog Number | 0035630 |
Lot Number | NGBN2305 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
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 | 2018-07-10 |