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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Stryker Instruments Div. of Stryker Corporation: Hairline fractures in a component could allow electrical current to arc out of the device, resulting in a burn to the patient and/or user.

Agency Publication Date: January 28, 2020
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Affected Products

Product: SafeAir Telescopic Smoke Evacuation Pencil, Product No. 0703 046 004. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332

1921032

Product: Telescopic Smoke Evac Pencil, PB, Coated, Product No. SHKTSPCL. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332

1923011, 1923050, 1924004, 1924005, 1924015, 1929038, 1929039, 1929055

Product: Telescopic Uncoated (Push Button), Product No. SHK TSPL. The product is a Bovie pencil that is 75 inches long compressed, with a telescoping shaft. UDI GTIN 37613327466332

1922042, 1924003, 1929040, 1929048

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84721
Status: Resolved
Manufacturer: Stryker Instruments Div. of Stryker Corporation
Manufactured In: United States
Units Affected: 3 products (15150)
Agency Last Updated: February 6, 2020

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.