Neptune E-SEP 165mm Blade Electrode — Class II medical device recall Z-1807-2020
Terminated recall by Stryker Instruments Div. of Stryker Corporation, reported 2020-05-06. Due to a distribution error, product from the affected lot was shipped expired.
| Recall number | Z-1807-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker Instruments Div. of Stryker Corporation, Portage, MI, United States |
| Recall initiated | 2020-03-26 |
| Classified | 2020-04-28 |
| Reported by FDA | 2020-05-06 |
| Terminated | 2020-07-15 |
| Countries outside the US | CA |
| Quantity | 40 units |
| UPC / GTIN / UDI-DI | 07613327297799 |
| Lot numbers | 16240231 |
| Model numbers | 0703-165-001 |
Product
Neptune E-SEP 165mm Blade Electrode, Catalog Number 0703-165-001 - Product Usage: The Neptune E-SEP is an Integrated Smoke Evacuation Pencil (pencil) designed for general electrosurgical applications including cutting and coagulation, and for removing smoke generated by electrosurgery when used in conjunction with an effective smoke evacuation system.
Reason for recall
Due to a distribution error, product from the affected lot was shipped expired.
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-1807-2020. 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.