FDA Device recall Z-1936-2013
C-QUR Mesh (All Sizes, shapes)
- FDA Device
- Class II
- terminated
- Published 2013-08-21
On 2013-08-21 the FDA classified a Class II recall of C-QUR Mesh (All Sizes, shapes) by Atrium Medical, citing additional Instructions for Use and Storage Conditions as Coated mesh can adhere to the inner packaging liner due to exposure to high humidity conditions.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1936-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-07-19 |
| Published | 2013-08-21 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Atrium Medical |
| Distribution | US |
Product
C-QUR Mesh (All Sizes, shapes). Intended for use in soft tissue deficiencies.
Reason
Additional Instructions for Use and Storage Conditions as Coated mesh can adhere to the inner packaging liner due to exposure to high humidity conditions
Identifiers
| code_info | Product lines with lot number 10405513 and higher |
|---|
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-1936-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.