Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

© 2026 Go Backs. All rights reserved.

High RiskFDA Vet
Medical Devices

Arizant Inc: Medical Power Cords Recalled Due to Potential Fire and Shock Hazards

Agency Publication Date: March 2, 2010
Share:
Sign in to monitor this recall

Summary

Arizant Inc. has initiated a nationwide recall of approximately 169,074 100/110-volt power cords (part number 502221, model 90024) used with several medical temperature management and infusion units. These cords are attached to devices including the Bair Hugger Models 500/OR, 505, 750, and 775, Bair Paws Models 850 and 875, and Ranger Blood/Fluid warming units. The recall was initiated because the power cords can fail, posing potential electrical or safety risks to both human and veterinary patients.

Risk

The power cords may experience electrical failure or degradation, which can lead to overheating, sparks, or fire, potentially causing burns or electrical shock during medical procedures.

What You Should Do

  1. Identify if your device uses the affected 100/110-volt power cord by checking for Arizant part number 502221 and Model number 90024.
  2. Check the model of your temperature management or infusion unit to see if it is a Bair Paws Model 850 or 875; a Bair Hugger Model 500/OR, 505, 750, or 775; or a Ranger Blood/Fluid Warming Unit Model 245.
  3. Immediately inspect the power cord for any signs of wear, fraying, or heat damage, and contact the manufacturer to determine if a replacement cord is required.
  4. Contact Arizant Healthcare Inc. directly at their Eden Prairie, Minnesota headquarters by calling 1-800-733-7775 for specific instructions on cord replacement or unit servicing.
  5. If you are a veterinary or medical professional, contact your healthcare provider or the manufacturer for further instructions regarding the continued use of these devices and potential refunds or replacements.
  6. For additional questions, you may contact the FDA's consumer hotline at 1-888-INFO-FDA (1-888-463-6332).

Your Remedy Options

📋Other Action

Manufacturer initiated voluntary recall for power cords

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

Affected Products

Product: Electri-Cord AC power cords for Bair Hugger Temperature Management Units
Model:
Model 505
Model 750
Arizant part number 502221
Model 90024
Lot Numbers:
Recall #: V-038-2010
Product: Electri-Cord AC power cords for Ranger Blood/Fluid Warming Units
Model:
Model 245
Arizant part number 502221
Model 90024
Lot Numbers:
Recall #: V-039-2010
Product: Bair Paws Temperature Management Units
Model:
Model 850
Model 875
Arizant part number 502221
Model 90024
Product: Bair Hugger Temperature Management Units
Model:
Model 500/OR
Model 775
Arizant part number 502221
Model 90024

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 54516
Status: Resolved
Manufacturer: Arizant Inc
Sold By: Arizant Healthcare Inc.; Medical supply distributors
Manufactured In: United States
Units Affected: 2 products (Total distributed for all devices: 84,537 US, 7,380 OUS.)
Distributed To: Nationwide

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