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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 Vet
Medical Devices/Monitoring Devices

Smiths Medical PM, Inc.: Surgivet Advisor Vital Signs Monitor Recalled for Mounting Bracket Failure

Agency Publication Date: April 24, 2009
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Summary

Smiths Medical PM, Inc. has recalled 196 units of the Smiths Medical Surgivet Advisor Vital Signs Monitor, Model 9200, due to a manufacturing defect in the monitor's plastic casing. A change made in July 2008 caused mounting inserts to be embedded too deeply into the plastic, preventing the monitor from being properly secured to wall mount brackets or roll stands. Approximately 165 units were distributed in the United States and 31 units were distributed internationally. Owners should contact the manufacturer or their healthcare provider immediately to address the mounting issue.

Risk

The defect prevents the vital signs monitor from being securely attached to its mounting hardware. If the monitor is not properly secured, it could fall from a wall mount or roll stand, potentially causing injury to staff or patients or damaging the device, which could lead to a loss of patient monitoring capabilities.

What You Should Do

  1. Identify your device by checking for the Smiths Medical Surgivet Advisor Vital Signs Monitor, Model 9200, which is involved in Recall Number V-138-2009.
  2. Inspect the back of the monitor to determine if it is securely fastened to its wall mount bracket or roll stand bracket, specifically if it was manufactured or modified after July 2008.
  3. If the monitor appears loose or cannot be properly secured to the mounting hardware, contact your healthcare provider or Smiths Medical PM, Inc. at their Waukesha, Wisconsin facility to discuss repair or replacement options.
  4. Contact the manufacturer at their facility located at N7 W22025 Johnson Dr, Waukesha, WI 53186-1856, for further instructions regarding this hardware defect.
  5. For additional questions or to report issues, contact the FDA’s consumer complaint coordinator or the general FDA hotline at 1-888-463-6332.

Your Remedy Options

📋Other Action

Manufacturer notification and potential hardware correction

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Smiths Medical Surgivet Advisor Vital Signs Monitor, Model 9200
Model:
Model 9200
V-138-2009
Date Ranges: Units manufactured or modified starting July 2008

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 51810
Status: Resolved
Manufacturer: Smiths Medical PM, Inc.
Sold By: Medical equipment distributors
Manufactured In: United States
Units Affected: 196 (165 US, 31 OUS)
Distributed To: Alabama, Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Nevada, New Jersey, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Texas, Virginia, Washington, Wisconsin

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.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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