FDA Device recall Z-0155-2015
Coloplast Conveen Urine Collection Leg Bag, Product Numbers 5170, 5171, and 5174
- FDA Device
- Class II
- terminated
- Published 2014-11-05
On 2014-11-05 the FDA classified a Class II recall of Coloplast Conveen Urine Collection Leg Bag, Product Numbers 5170, 5171, and 5174 by Coloplast Manufacturing Us, citing coloplast is recalling the Conveen Contour Leg Bag due to potential leakage from the bag seam when filled.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0155-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-09-29 |
| Published | 2014-11-05 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Coloplast Manufacturing Us |
| Distribution | US |
Product
Coloplast Conveen Urine Collection Leg Bag, Product Numbers 5170, 5171, and 5174. Urine Collection Bag.
Reason
Coloplast is recalling the Conveen Contour Leg Bag due to potential leakage from the bag seam when filled.
Identifiers
| code_info | Lot Numbers: 3880261, 3880268, 3932929, 3932933, 3940329, 3940332, 3949825, 3949828, 3968997, 3969002, 3997492, 399777…Lot Numbers: 3880261, 3880268, 3932929, 3932933, 3940329, 3940332, 3949825, 3949828, 3968997, 3969002, 3997492, 3997778, 3997782, 4006822, 4019572, 4019574, 4047072, 4047075, 4056422, 4056423, 4056428, 4073930, 4073934, 4092990, 4092991, 4100228. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0155-2015%22
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