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.

Medium RiskFDA Device

St. Jude Medical, Cardiac Rhythm Management Division: There is a potential for programmer software (Merlin PCS) and remote monitoring software application (Merlin.net) to display overestimated predicted battery longevity for certain pacemakers.; The Merlin" 2 PCS model MER3700 is a portable, dedicated programming system designed to interrogate, program, display data from, and test Abbott Medical implantable medical devices during implant and follow-up.

Agency Publication Date: August 2, 2022
Share:
Sign in to monitor this recall

Affected Products

Product: Merlin PCS 3650 programmer Model 3330 software

Software Model 3330 v26.0.1 rev 1 or earlier; UDI/DI 05414734509725

Product: Merlin 2 PCS MER37000 programmer Model MER3400 software

Software Model MER3400 v1.1.2 rev 1 or earlier.; UDI/DI 05415067037121

Product: Merlin.net model MN5000 Software

Software Merlin.net" v11.7 (MN5000 v7.8.rev6).; UDI/DI 05414734509732

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90530
Status: Active
Manufacturer: St. Jude Medical, Cardiac Rhythm Management Division
Manufactured In: United States
Units Affected: 3 products (29,996 programs; 622 programs; unknown)

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

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.