Reported Nov 20, 2024 · Ongoing

Stryker Neptune SafeAir Smoke Evacuation Pencil Coated Rocker-Switch, Bulk Non-Sterile - Designed for general…

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 Smoke Evacuation Pencil Coated Rocker-Switch, Bulk Non-Sterile - 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 Number0703-047-002
Lot codes and dates
  • GTIN07613327379471
  • Lot Numbers
    • 53700305
    • 53864207
    • 53864241
    • 53864247
    • 60308905
    • 62012084
    • 64112630
    • 65342955
    • 53700306
    • 53864212
    • 53864243
    • 53864248
    • 60308906
    • 62291715
    • 64112631
    • 65869470
    • 53700307
    • 53864213
    • 53864244
    • 53864249
    • 60308907
    • 62291717
    • 64142443
    • 65869471
    • 53700308
    • 53864214
    • 53864245
    • 53864257
    • 61283868
    • 62821201
    • 64968515
    • 65954806
    • 53864205
    • 53864219
    • 53864246
    • 60308904
    • 61283869
    • 64112629
    • 64968516
    • 66005707
    • 53864206
  • Additional Lot Numbers
    • 64917537
    • 65342956
    • 66487443
    • 67787272
    • 67840867
    • 68672644
    • 64917538
    • 66487442
    • 67787271
    • 67840866
    • 67840868
    • 68672645
Amount recalled
295,760 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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 6:46 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.