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

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/Monitoring Devices

GE Medical Systems, LLC: If a user incorrectly places the Acquisition Module into the Acquisition Module Holder, it can result in excessive bending and wear of the Acquisition Trunk Cable. This is visible as a damaged sheath or exposed wires. If a damaged Acquisition Trunk Cable is not recognized and removed from service, the cable can overheat with continued use.

Agency Publication Date: October 22, 2025
Share:
Sign in to monitor this recall

Summary

GE Medical Systems is recalling 29,225 units of the MAC VU360 Acquisition Trunk Cable and Module Holder used with resting electrocardiograph (ECG) machines. If the module is placed incorrectly into its holder, the cable can experience excessive bending and wear, leading to damaged insulation or exposed wires. If a damaged cable remains in use, it can overheat, posing a risk of fire or thermal injury. No incidents or injuries have been reported at this time. Consumers should inspect their equipment for visible damage and contact GE Medical Systems for further guidance.

Risk

The acquisition module holder design may allow for incorrect placement, which causes the trunk cable to bend sharply and wear down over time. This wear can expose internal wiring, which may lead to electrical overheating and potential burns or fires during medical procedures.

What You Should Do

  1. Check your device's model and serial number to see if it is included in the recall. Affected products include the MAC VU360 Acquisition Trunk Cable and Module Holder, Model Number 2030360-001, with serial numbers beginning with VU2 or VU4.
  2. Inspect the Acquisition Trunk Cable for any signs of a damaged outer sheath, fraying, or exposed internal wires.
  3. If any damage is found, immediately remove the damaged cable from service and do not use it on patients.
  4. Contact GE Medical Systems directly at 1-800-437-1171 or visit their website to report damaged components and receive instructions on obtaining a replacement or repair.
  5. Contact your healthcare provider if you have concerns about a recent procedure involving this equipment.
  6. For additional questions, contact the FDA at 1-888-463-6332 or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Manufacturer Notification and Inspection

How to: Contact your healthcare provider or the manufacturer (GE Medical Systems) for further instructions on equipment inspection and potential repair/replacement.

Affected Products

Product: MAC VU360 Acquisition Trunk Cable and Module Holder, high performance, multichannel resting electrocardiograph
Model / REF:
2030360-001
VU2
VU4
Lot Numbers (2327):
VU221240028SA
VU221250168SA
VU222120101SA
VU222120114SA
VU222120120SA
VU222400056SA
VU222400070SA
VU222480182SA
VU421010035SA
VU420530073SA
VU420530105SA
VU420530108SA
VU420530109SA
VU420530110SA
VU421010007SA
VU421010008SA
VU421010009SA
VU421010010SA
VU421010012SA
VU421010021SA
VU421010029SA
VU421010040SA
VU421010042SA
VU422410219SA
VU422410220SA
VU220500166SA
VU220500167SA
VU222250167SA
VU222250175SA
VU423290038SA
VU423290039SA
VU423290063SA
VU423290068SA
VU221500205SA
VU221500215SA
VU221500216SA
VU221500218SA
VU221300012SA
VU221320090SA
VU221330009SA
VU221330012SA
VU221330013SA
VU221120005SA
VU221490009SA
VU221490015SA
VU221490031SA
VU221490033SA
VU221490038SA
VU221490043SA
VU221490113SA

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97564
Status: Active
Manufacturer: GE Medical Systems, LLC
Manufactured In: United States
Units Affected: 29,225 units

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.