FDA Device recall Z-1509-2014
Monodek Violet Synthetic Absorbable Surgical Sutures, MF 0 TC43/HR26 48
- FDA Device
- Class II
- terminated
- Published 2014-04-30
On 2014-04-30 the FDA classified a Class II recall of Monodek Violet Synthetic Absorbable Surgical Sutures, MF 0 TC43/HR26 48 by Teleflex Medical, citing product does not meet minimum knot tensile strength requirements.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1509-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-03-11 |
| Published | 2014-04-30 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Teleflex Medical |
| Distribution | MA |
Product
Monodek Violet Synthetic Absorbable Surgical Sutures, MF 0 TC43/HR26 48
Reason
Product does not meet minimum knot tensile strength requirements.
Identifiers
| code_info | Product Code: 833-137, Batch: 02H1103434, 02H1200349, and 02K1201354. |
|---|
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-1509-2014%22
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