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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Implants & Prosthetics

Abbott Medical: Abbott Infinity Pulse Generators Recalled for Premature Battery Depletion

Agency Publication Date: July 25, 2024
Share:
Sign in to monitor this recall

Summary

Abbott Medical is recalling approximately 33,788 Infinity 5 and Infinity 7 Implantable Pulse Generators due to a defect where the battery life indicator and 'end of service' date may be shorter than stated in the product labeling. This unexpected battery depletion can cause the device to stop working sooner than anticipated, leading to a sudden loss of therapy for patients. Because these are implanted medical devices, consumers should not attempt to remove or modify the product themselves but must work closely with their medical team.

Risk

The defect causes the device's replacement indicator to trigger late or inaccurately, which can result in the device losing power and stopping therapy without sufficient warning to the patient. For patients relying on these pulse generators, a sudden loss of therapy can lead to a recurrence of symptoms or other serious health complications.

What You Should Do

  1. Identify if you have an affected device by checking your patient identification card for model numbers (REF) 6660, 6661, 6662, or 6663.
  2. Check your device's unique identifier or serial number against the following affected codes: 05415067030016, 05415067020246, 05415067020253, 05415067030023, 05415067020260, or 05415067020277.
  3. Contact your healthcare provider or cardiologist immediately to discuss the status of your implant and to determine if your device is reaching its end of service earlier than expected.
  4. Do not attempt to change any device settings or take any medical action without professional supervision.
  5. Contact Abbott Medical for further technical instructions or information regarding this recall.
  6. For additional questions or to report a problem, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Healthcare provider consultation

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

Affected Products

Product: Abbott Infinity 5, Implantable Pulse Generator, REF: 6660
Model / REF:
6660
UPC Codes:
05415067030016
05415067020246
Product: Abbott Infinity 5, Implantable Pulse Generator, REF: 6661
Model / REF:
6661
UPC Codes:
05415067020253
Product: Abbott Infinity 7, Implantable Pulse Generator, REF: 6662
Model / REF:
6662
UPC Codes:
05415067030023
05415067020260
Product: Abbott Infinity 7, Implantable Pulse Generator, REF: 6663
Model / REF:
6663
UPC Codes:
05415067020277

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 94796
Status: Active
Manufacturer: Abbott Medical
Sold By: Hospitals; Surgical Centers; Medical Professionals
Manufactured In: United States
Units Affected: 4 products (5,900 units; 5,900 units; 20,790 units; 1198 units)
Distributed To: Alabama, Arkansas, Arizona, California, Colorado, District of Columbia, Florida, Georgia, Illinois, Indiana, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Montana, North Carolina, North Dakota, Nebraska, New Hampshire, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, South Carolina, Texas, Utah, Virginia, Washington, Wisconsin, Wyoming

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

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.