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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: Hip liner implant boxes may contain knee inserts and knee insert boxes may contain hip liner implants, which may lead to implants not being available for surgeries, which may cause delays in surgery.

Agency Publication Date: October 21, 2022
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Affected Products

Product: EMPOWR Acetabular System, Liner, 10 deg Hooded, HXe+ 40H, REF: 942-01-40H. Orthopedic implant component.

UDI-DI/Lot: 00190446309833/629Z1085

Lot Numbers:
00190446309833
Product: EMPOWER 3D Knee Tibial Insert, REF: 341-14-708. Orthopedic implant component.

UDI-DI/Lot: 00888912167055/132T1085

Lot Numbers:
00888912167055

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 90882
Status: Active
Manufacturer: Encore Medical, LP
Manufactured In: United States
Units Affected: 2 products (4; 18)

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.