FDA Device recall Z-1239-2017
Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
- FDA Device
- Class II
- terminated
- Published 2017-03-01
On 2017-03-01 the FDA classified a Class II recall of Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701 by Smith And Nephew, citing the single use devices are provided sterile and do not have an expiration date on the label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1239-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-02-02 |
| Published | 2017-03-01 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Smith And Nephew |
| Distribution | US |
Product
Smith & Nephew Dyonics Saw Blade, Standard, Product Number 3701
Reason
The single use devices are provided sterile and do not have an expiration date on the label.
Identifiers
| code_info | Batch Numbers: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 501…Batch Numbers: 50586138 50458123 50418120 50339534 50306882 50285907 50248565 50231427 50197615 50171397 50158655 50138049 50119457 50089297 50082581 50069485 |
|---|
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-1239-2017%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.