Reported Nov 20, 2024 · Ongoing
Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Coated, 70mm - Designed for general electrosurgical…
Stryker Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Stryker Corporation · 1941 Stryker Way · Portage, MI · 49002-9711
Is this the product you have?
- Stryker Neptune SafeAir Rocker-Switch Smoke Evacuation Pencil, Coated, 70mm - 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
- Catalog Number0703-047-000
- Lot codes and dates
- UDI-DI07613327117202
- Lot Numbers
147 of 147 codes
538636665440985956319954569456535769937559053479651789455386366754409860563199555694565457699376590534806517894653863668544098625631995657699353576993775905348165178947538636695440991956319957576993545769937859053482651789495386367054409920563199585769935557699379590534836534799753863671544099215631995957699359576993806128893765784636544039595440992256319960576993605769938161288943657846375440396054409923563199615769936157699382628257816578463854403961544099245689267657699362
- V53934893 Additional Lot Numbers
6426256666387346665992516675865467377504676526116779451464973268663873476670554966758655673775056765261268735135651789526638734866705550670176756737750667652613687351366517895366387349667586526701767667481713677945126873513766387345665992506675865367207470676526106779451368735138
- Amount recalled
- 1,120,860 eaches
This recall covers 6 products
The agency filed one notice per product. You are reading one of them; the other 5 are below.
Where it was sold
- Nationwide
Why it was recalled
There is a potential for the product to activate without manual input when plugged into a power source or remain active after buttons are released. Unintentional activation of the device may result in localized burns to the patient or physician from electrical currents carried through conductive objects or fluids. Medical/surgical intervention may be needed to correct these injuries
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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