D-RAD — Class II medical device recall Z-1856-2017
Terminated recall by Smith & Nephew, Inc., reported 2017-04-26, distributed nationwide. The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the lab
| Recall number | Z-1856-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Smith & Nephew, Inc., Memphis, TN, United States |
| Recall initiated | 2017-03-09 |
| Classified | 2017-04-18 |
| Reported by FDA | 2017-04-26 |
| Terminated | 2019-08-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | CO, DK, FI, FR, GB, IT, SG |
| Quantity | 100 units |
| Reason classes | labeling |
| Lot numbers | 14MM07780R |
Product
D-RAD, 2.4MMX 20MM, S.T. CORTEX SCREW, QTY: (1), STERILE R, RES 74682420 Orthopedic
Reason for recall
The expiration dates on the labeling are incorrect, the actual expiration dates are before the date on the labeling.
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-1856-2017. 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.