MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 08 report with the FDA on 2010-10-06 for (OUT)LEG BAG 950 ML UB09501400 manufactured by Coloplast Manufacturing Us, Llc.
[1702496]
(b)(4)date of event: best estimate is (b)(6)2010according to the information recieved, a complaint was received for blocked urineflow. An end user stated that a bag clogs which keeps the bag from draining.
Patient Sequence No: 1, Text Type: D, B5
[8770731]
Information received indicated there are no samples to return for evaluation. Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurence. Should the device or additional information be received, a follow up report will be filed.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2183558-2010-00038 |
| MDR Report Key | 1857350 |
| Report Source | 08 |
| Date Received | 2010-10-06 |
| Date of Report | 2010-09-09 |
| Date Mfgr Received | 2010-09-09 |
| Date Added to Maude | 2010-10-07 |
| 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 | MR. BRIAN SCHMIDT |
| Manufacturer Street | 1601 WEST RIVER ROAD NORTH |
| Manufacturer City | MINNEAPOLIS MN 55411 |
| Manufacturer Country | US |
| Manufacturer Postal | 55411 |
| Manufacturer Phone | 6123024987 |
| Manufacturer G1 | COLOPLAST MANUFACTURING US, LLC |
| Manufacturer Street | 1185 WILLOW LAKE BLVD |
| Manufacturer City | VADNAIS HEIGHTS, MN 55110 55110 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 55110 |
| Single Use | 0 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | (OUT)LEG BAG 950 ML |
| Generic Name | URINE LEG BAG |
| Product Code | NNW |
| Date Received | 2010-10-06 |
| Model Number | UB09501400 |
| Catalog Number | UB09501400 |
| Operator | LAY USER/PATIENT |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COLOPLAST MANUFACTURING US, LLC |
| Manufacturer Address | 1185 WILLOW LAKE BLVD. VADNAIS HEIGHTS MN 55110 US 55110 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2010-10-06 |