MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,05,06 report with the FDA on 2015-01-16 for UNOMETER SAFETI PLUS - WITH LUER-LOCK AND LUER 158101310190 manufactured by Unomedical Ltd..
[5393610]
It was reported the urinometer was attached to the patient's catheter; when the patient was turned, approximately 2 hours later, the nurse noted the urinometer had become detached from the catheter. As a result, the patient's bed linens were wet. The urinometer was discontinued at that time and replaced with a leg bag.
Patient Sequence No: 1, Text Type: D, B5
[12849546]
Based on the available information, this event is deemed a reportable malfunction. There were no reports of the patient being harmed as a result of this malfunction. No additional patient/event details were available at the time of this report. Should additional information becomes available, a follow-up report will be submitted.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3007966929-2015-00021 |
MDR Report Key | 4432415 |
Report Source | 01,05,06 |
Date Received | 2015-01-16 |
Date of Report | 2015-01-05 |
Date of Event | 2014-12-23 |
Date Mfgr Received | 2015-01-05 |
Device Manufacturer Date | 2014-09-01 |
Date Added to Maude | 2015-02-05 |
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 | MATTHEW WALENCIAK, INTERIM ASSOC. |
Manufacturer Street | 211 AMERICAN AVE. |
Manufacturer City | GREENSBORO NC 27409 |
Manufacturer Country | US |
Manufacturer Postal | 27409 |
Manufacturer Phone | 9083779293 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | UNOMETER SAFETI PLUS - WITH LUER-LOCK AND LUER |
Generic Name | URINOMETER, MECHANICAL |
Product Code | EXR |
Date Received | 2015-01-16 |
Model Number | 158101310190 |
Lot Number | 170548 |
Device Expiration Date | 2019-08-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | UNOMEDICAL LTD. |
Manufacturer Address | ZAVODSKAYA STREET 50 FANIPOL DZERZHINSK DISTRICT MINSK REGION 222750 BO 222750 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-01-16 |