MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2002-06-14 for DRAINAGE BAG WITH REFLUX VALVE DYNC1674 * manufactured by Medline Industries, Inc..
[269130]
Reportedly two pt's contracted urinary tract infections because the drainage bags did not drain properly. The pt's were treated with antibiotics. No further medical treatment was required.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1417592-2002-00008 |
MDR Report Key | 399911 |
Report Source | 07 |
Date Received | 2002-06-14 |
Date of Report | 2002-06-14 |
Date of Event | 2002-05-17 |
Date Mfgr Received | 2002-05-17 |
Device Manufacturer Date | 2001-10-01 |
Date Added to Maude | 2002-06-19 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | ANDREA HAFERKAMP |
Manufacturer Street | ONE MEDLINE PL |
Manufacturer City | MUNDELEIN IL 60060 |
Manufacturer Country | US |
Manufacturer Postal | 60060 |
Manufacturer Phone | 8478372759 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DRAINAGE BAG WITH REFLUX VALVE |
Generic Name | URINE COLLECTOR |
Product Code | EYZ |
Date Received | 2002-06-14 |
Model Number | DYNC1674 |
Catalog Number | * |
Lot Number | 102801AZ101 |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 388956 |
Manufacturer | MEDLINE INDUSTRIES, INC. |
Manufacturer Address | ONE MEDLINE PL. MUNDELEIN IL 60060 US |
Baseline Brand Name | DRAINAGE BAG W/REFLUX VALVE |
Baseline Generic Name | URINE COLLECTOR |
Baseline Model No | DYNC1674 |
Baseline Device Family | DN11 |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2002-06-14 |