FDA Device recall Z-1244-2017
Smith & Nephew Dyonics Saw Blade, Long, Special, Product Number 3706
- 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, Long, Special, Product Number 3706 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-1244-2017 |
| 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, Long, Special, Product Number 3706
Reason
The single use devices are provided sterile and do not have an expiration date on the label.
Identifiers
| code_info | Batch Numbers: 50439354 50393992 50252777 50208023 50171402 50138054 50103142 50066114 576304 |
|---|
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-1244-2017%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.