FDA Device recall Z-1939-2013
C-QUR TacShield Mesh (All sizes and shapes)
- FDA Device
- Class II
- terminated
- Published 2013-08-21
On 2013-08-21 the FDA classified a Class II recall of C-QUR TacShield Mesh (All sizes and 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-1939-2013 |
| 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 TacShield Mesh (All sizes and 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-1939-2013%22
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