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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

DePuy Orthopaedics, Inc.: The subject product lots are being recalled because they received a higher than specified irradiation dose. This exceeds the validated range for exposure to gamma radiation of these devices and may result in changes to the implant material properties.

Agency Publication Date: March 17, 2023
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Affected Products

Product: Attune Revision Limb Preservation System (LPS) Tibial Insert XXSM 18MM, Part Number 151760118

GTIN: 10603295491095; Lot: JP6452

Lot Numbers:
JP6452
Product: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 12MM, Part Number 151760212

GTIN: 10603295490968; Lot: JP9016

Lot Numbers:
JP9016
Product: Attune Revision Limb Preservation System (LPS) Tibial Insert XSM 26MM, Part Number 151760226

GTIN: 10603295491033; Lot: JP9022

Lot Numbers:
JP9022
Product: Attune Revision Limb Preservation System (LPS) Tibial Insert SM 12MM, Part Number 151760312

GTIN: 10603295490869; Lot: JP6464

Lot Numbers:
JP6464
Product: Attune Posterior (PS) Fixed Bearing (FB) Tibial Insert SZ5 7MM, Part Number 151640507

GTIN: 10603295049944; Lot: JN6613

Lot Numbers:
JN6613

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91752
Status: Active
Manufacturer: DePuy Orthopaedics, Inc.
Manufactured In: United States
Units Affected: 5 products (7 units; 7 units; 7 units; 7 units; 12 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.