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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

Microline Surgical, Inc.: Potential for the Fenestrated Grasper Tip jaw to break when force is applied to the jaw

Agency Publication Date: July 2, 2014
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Affected Products

Product: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips Ref 3221

Lot Numbers: 00115342

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Product: Microline Surgical ReNew Laproscopic Fenestrated Grasper Forceps Tips (Reusable) Ref 3222

Lot Numbers: Lot Number 00115282 Lot Number 00115283 Lot Number 00115284 Lot Number 00115340 Lot Number 00115341 Lot Number 00115501 Lot Number 00115502 Lot Number 00115865 Lot Number 00116277 Lot Number 00116278

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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 68495
Status: Resolved
Manufacturer: Microline Surgical, Inc.
Manufactured In: United States
Units Affected: 2 products (150 units; 6290 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.

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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.