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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

Encore Medical, LP: There have been issues experienced with the peg preparation steps, specifically drilling of the Femoral posterior peg. Upon drilling, the shaft portion of the drill may bind within the Posterior Peg drill guide. The extended length of the drill guide and tight tolerances to ensure accurate preparation seem to be contributing to this situation. There is a potential of a delay in surgery if this issue were to recur.

Agency Publication Date: November 20, 2020
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Affected Products

Product: EMPOWR Partial Knee Peg Drill Guide; Model: 800-06-007.

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Lot Numbers:
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Product: EMPOWR Partial Knee Peg Drill; Model: 800-06-008.

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Lot Numbers:
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Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 85943
Status: Active
Manufacturer: Encore Medical, LP
Manufactured In: United States
Units Affected: 2 products (28 units)

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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.