C-QUR V-Patch Mesh — Class II medical device recall Z-1938-2013
Terminated recall by Atrium Medical Corporation, reported 2013-08-21, distributed nationwide. Additional Instructions for Use and Storage Conditions as Coated mesh can adhere to the inner packaging liner
| Recall number | Z-1938-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Atrium Medical Corporation, Hudson, NH, United States |
| Recall initiated | 2013-07-19 |
| Classified | 2013-08-09 |
| Reported by FDA | 2013-08-21 |
| Terminated | 2016-03-18 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BH, BR, CA, CH, CL, CO, DE, DO, EC, ES, FR, GB, GR, HK, HN, IE, IL, IN, IT, JO, JP, KR, LK, MX, MY, NI, NL, NO, NZ, PA, PE, PT, RO, SA, SG, SV, TH, TR, TW, VE, ZA |
| Quantity | 95,286 units |
| Lot numbers | 10405513 |
Product
C-QUR V-Patch Mesh (All sizes and shapes). Intended for use in soft tissue deficiencies.
Reason for recall
Additional Instructions for Use and Storage Conditions as Coated mesh can adhere to the inner packaging liner due to exposure to high humidity conditions
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1938-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.