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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

Bausch & Lomb Inc Irb: Possible dull knife edge

Agency Publication Date: August 24, 2019
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Affected Products

Product: Laseredge Knife 1.5mm X 1.7mm TRAPEZOID ANGLED, REF E7599 Product Usage: Available to surgeons for use in ophthalmic surgical procedures.

Lot Number: MAXZ170 Expiry Date: 01/28/2021

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 74671
Status: Resolved
Manufacturer: Bausch & Lomb Inc Irb
Manufactured In: United States
Units Affected: 165 packs/6 blades (990 individiual blades)

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.