PlainRecalls
FDA Devices Moderate Class II Terminated

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.

Reported: May 6, 2020 Initiated: March 26, 2020 #Z-1807-2020

Product Description

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.

Details

Units Affected
40 units
Distribution
International distribution the country of Canada.
Location
Portage, MI

Frequently Asked Questions

What product was recalled?
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.. Recalled by Stryker Instruments Div. of Stryker Corporation. Units affected: 40 units.
Why was this product recalled?
Due to a distribution error, product from the affected lot was shipped expired.
Which agency issued this recall?
This recall was issued by the FDA Devices on May 6, 2020. Severity: Moderate. Recall number: Z-1807-2020.