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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

Zimmer Biomet, Inc.: Possibility that the patient label inside the product box was incorrectly labeled. The outer box label and actual product are correctly identified but the internal patient label could be incorrect.

Agency Publication Date: December 29, 2017
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Affected Products

Product: Lateral Troch Plate Full Crimp - 254mm, model # 350837

Lot Number: 340530

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Product: Lateral Troch Plate Full Crimp - 254mm, model # 350838

Lot Number: 406590

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Product: COMP 12MM HUM FRAC STEM MACRO, model # 11-113562

Lot Number: 529890

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Number
Product: COMP PRIMARY STEM 8MM MINI, model # 113628

Lot Number: 523080

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Number
Product: ECHO POR FMRL NC 9X125, model # 192009

Lot Number: 410150

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Number
Product: CER OPTION TYPE 1 TPR SLEVE -6, model # 650-1064

Lot Number: 854540

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Number
Product: CER BIOLOXD OPTION HD 32MM, model # 650-1056

Lot Number: 843260

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Number
Product: OSS CEMENTED IM STEM 12X150, model # 150366

Lot Number: 71180

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Number
Product: RED SEXP DSTL FEM 19CM RT ASSY, model # CP111817

Lot Number: 856460

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Number
Product: RED SEXP DSTL FEM 19CM LT ASSY, model # CP111828

Lot Number: 856550

Lot Numbers:
Number

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 78167
Status: Resolved
Manufacturer: Zimmer Biomet, Inc.
Manufactured In: United States

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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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

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.