FDA Device recall Z-2603-2016
TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030
- FDA Device
- Class II
- terminated
- Published 2016-08-31
On 2016-08-31 the FDA classified a Class II recall of TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030 by Novus Scientific Ab, citing novus Scientific is implementing additions to the product's instructions for use concerning certain inguinal hernia repairs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2603-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-19 |
| Published | 2016-08-31 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Novus Scientific Ab |
| Distribution | CA, FL, IL, KY, MO, NC, NH, NY, OH, TN, TX, VA |
Product
TIGR Matrix Surgical Mesh, Model No. NSTM1015, NSTM1520, NSTM2030
Reason
Novus Scientific is implementing additions to the product's instructions for use concerning certain inguinal hernia repairs.
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2603-2016%22
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