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.

Critical RiskFDA Device
Medical Devices/Surgical Equipment

Mercury Enterprises, Inc. dba Mercury Medical: Neo-Tee T-Piece Resuscitator Recalled for Potential Circuit Failure

Agency Publication Date: October 2, 2024
Share:
Sign in to monitor this recall

Summary

Mercury Medical is recalling 1,300 units of the Neo-Tee T-Piece Resuscitator, models 1050805 and 1050832, used for pediatric emergency respiratory support. The recall was initiated because a critical manufacturing step was missed, which may cause the manual resuscitator's circuit flow controller to come apart during use. This defect can interrupt life-saving respiratory support for infants and children in emergency situations.

Risk

If the flow controller detaches while the device is in use, the patient may not receive necessary oxygen or ventilation. This poses a significant risk of respiratory failure, oxygen deprivation, and other life-threatening complications for pediatric patients requiring emergency breathing assistance.

What You Should Do

  1. Immediately check your medical supplies for Neo-Tee T-Piece Resuscitator Part Numbers 1050805 and 1050832.
  2. Verify the lot numbers on your devices. Affected lot numbers for Part Number 1050805 are 2417650805 and 2417750805. Affected lot numbers for Part Number 1050832 are 2423550832 and 2417850832.
  3. Identify the device by checking the UDI/DI codes: 10641043508053 or 30641043508057 (for Part 1050805) and 10641043508329 or 30641043508323 (for Part 1050832).
  4. If you possess an affected device, stop using it immediately and secure it to prevent use in an emergency.
  5. Contact Mercury Medical or your healthcare provider for specific instructions on returning the defective units and obtaining replacements.
  6. For further questions or technical support, contact Mercury Medical or call the FDA's medical device recall line at 1-888-463-6332.

Your Remedy Options

๐Ÿ“‹Other Action

Contact healthcare provider or manufacturer

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

Affected Products

Product: Neo-Tee T-Piece Resuscitator (Part Number 1050805)
Model / REF:
1050805
UPC Codes:
10641043508053
30641043508057
Lot Numbers:
2417650805
2417750805
Product: Neo-Tee T-Piece Resuscitator (Part Number 1050832)
Model / REF:
1050832
UPC Codes:
10641043508329
30641043508323
Lot Numbers:
2423550832
2417850832

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95303
Status: Active
Manufacturer: Mercury Enterprises, Inc. dba Mercury Medical
Sold By: Medical supply distributors
Manufactured In: United States
Units Affected: 1,300 units
Distributed To: Michigan, Florida, South Carolina, Pennsylvania, Indiana

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.