TIGR Matrix Surgical Mesh — Class II medical device recall Z-2603-2016
Terminated recall by Novus Scientific Ab, reported 2016-08-31, distributed in CA, FL, IL, KY, MO, NC, NH, NY…. Novus Scientific is implementing additions to the product's instructions for use concerning certain inguinal h
| Recall number | Z-2603-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Novus Scientific Ab, Uppsala, Sweden |
| Recall initiated | 2016-07-19 |
| Classified | 2016-08-19 |
| Reported by FDA | 2016-08-31 |
| Terminated | 2016-12-23 |
| Distributed | CA, FL, IL, KY, MO, NC, NH, NY, OH, TN, TX, VA |
| Countries outside the US | AT, BE, BG, CH, DE, DK, ES, FI, FR, GB, IE, IL, IR, IT, MT, NL, NO, NZ, PL, SE, SG, TR, ZA |
| Model numbers | NSTM1015, NSTM1520, NSTM2030 |
Product
TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030
Reason for recall
Novus Scientific is implementing additions to the product's instructions for use concerning certain inguinal hernia repairs.
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-2603-2016. 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.