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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.

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Medium RiskFDA Device
Medical Devices/Surgical Equipment

MST Duet Reusable Handles Recalled Due to Potential Pin Detachment

Agency Publication Date: November 22, 2024
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Summary

MicroSurgical Technology Inc is recalling approximately 24 MST Duet Reusable Handles for Single Use Heads because a pin on the handle can detach. This recall affects Model DFH-1028, specifically lot 160458. These reusable handles are used by surgeons during ophthalmic procedures with interchangeable forceps or scissor heads. While no injuries or incidents have been reported to date, the manufacturer is initiating this voluntary recall to prevent potential surgical complications. The company notified affected customers via letter.

Risk

If the pin detaches during a surgical procedure, it could fall into the patient's surgical site or cause the instrument to fail, potentially leading to eye injury, surgical delays, or the need for additional medical intervention.

What You Should Do

  1. This recall affects the MST Duet Reusable Handle for Single Use Heads (Model DFH-1028) with Lot Number 160458 and UDI 00844685005536.
  2. Stop using the recalled device immediately.
  3. Contact MicroSurgical Technology Inc or your authorized distributor to arrange for the return, replacement, or correction of the handle.
  4. Call the FDA at 1-888-463-6332 (1-888-INFO-FDA) for additional information regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: MST Duet Reusable Handle for Single Use Heads (Forceps and Scissors)
Model / REF:
DFH-1028
Lot Numbers:
160458
UDI:
00844685005536

Product Codes HNF or HNR (Regulation Number 886.4350) may apply as the handle can be used with both scissors and forceps heads.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95572
Status: Active
Manufacturer: MicroSurgical Technology Inc
Sold By: MicroSurgical Technology Inc
Manufactured In: United States
Units Affected: 24
Distributed To: Connecticut, Georgia, Minnesota, Montana, Texas

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.