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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.: Medical Device AC Power Cords Recalled Due to Electrical Concerns

Agency Publication Date: February 16, 2010
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Summary

Smiths Medical is recalling approximately 4,074 AC power cords manufactured by Electri-Cord Manufacturing Co. these cords were distributed for use with various medical devices, including the BCI 3180 Pulse Oximeter, 9200 Advisor Vital Signs Monitor, 8400 Capnocheck II Capnometer, and V6400 Invasive Pressure Monitor. The recall covers 1,358 specific cords distributed for all devices, including 1,032 in the United States. These power cords are used for both human and veterinary medical monitoring equipment.

Risk

The power cords may be defective, which could lead to a loss of power for critical vital signs monitoring equipment or pose an electrical hazard. While specific incidents are not detailed, any power failure in these monitoring devices could delay necessary medical intervention for human or animal patients.

What You Should Do

  1. Identify if your device uses an affected Electri-Cord power cord by checking for part numbers WW3005 or 8404.
  2. Check your device model to see if it is one of the following: BCI 3180 Pulse Oximeter, 9200 Advisor Vital Signs Monitor, 8400 Capnocheck II Capnometer, or V6400 Invasive Pressure Monitor.
  3. Immediately contact Smiths Medical PM, Inc. at their Waukesha, Wisconsin headquarters to determine if your specific serial number or cord batch is included in the recall and to arrange for a safe replacement.
  4. If you are a healthcare provider or veterinarian, contact Smiths Medical or your device distributor to verify the safety of your current power equipment.
  5. For further questions or to report issues, contact the FDA at 1-888-INFO-FDA (1-888-463-6332).

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer-led voluntary recall of equipment

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

Affected Products

Product: V6400 Invasive Pressure Monitor Power Cord
Model:
WW3005
Lot Numbers:
Recall #: V-033-2010
Product: V9200 Advisor Vital Signs Monitor Power Cord
Model:
WW3005
Lot Numbers:
Recall #: V-034-2010
Product: V8400 Capnocheck Capnometer Power Cord (Battery Charger)
Model:
8404
Lot Numbers:
Recall #: V-035-2010
Product: BCI 3180 Pulse Oximeter Power Cord

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 54361
Status: Resolved
Manufacturer: Smiths Medical PM, Inc.
Sold By: Smiths Medical PM, Inc.; Electri-Cord Manufacturing Co.
Manufactured In: United States
Units Affected: 3 products (1358 cords for all devices (1032 US, 326 OUS) (871 Human, 487 Vet), (Cord # 8404 5 Vet & 325 Human), (Cord # WW3005 482 Vet & 546 Human))
Distributed To: District of Columbia, Colorado, California, Wisconsin, Alabama, New York, Ohio, Florida, Maryland, New Hampshire, New Jersey, Michigan, Illinois, Missouri, Arizona, Indiana, Rhode Island, Pennsylvania, Oregon, Alaska, Idaho, North Carolina, Texas, Nevada, Connecticut, Georgia, Virginia, Arkansas, Massachusetts, Oklahoma, Tennessee, South Carolina, Minnesota, Hawaii, Utah, New Mexico, Washington

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 ยท Raw API Response