Smith & Nephew Dyonics Saw Blade — Class II medical device recall Z-1242-2017
Terminated recall by Smith & Nephew, Inc., reported 2017-03-01, distributed nationwide. The single use devices are provided sterile and do not have an expiration date on the label.
| Recall number | Z-1242-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2017-02-02 |
| Classified | 2017-02-22 |
| Reported by FDA | 2017-03-01 |
| Terminated | 2019-09-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | BR, CA, CL, CN, DK, HK, IN, MX, PE, SG, VE |
| Quantity | 8,748 |
| Reason classes | labeling, sterility |
| Lot numbers | 50061131, 50082582, 50089298, 50103379, 50121538, 50138050, 50158656, 50171398, 50178740, 50197616, 50261802, 50386077, 50525150 |
Product
Smith & Nephew Dyonics Saw Blade, Short, Narrow, Product Number 3704
Reason for recall
The single use devices are provided sterile and do not have an expiration date on the label.
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-1242-2017. 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.