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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

Corin Ltd: The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.

Agency Publication Date: December 19, 2022
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Affected Products

Product: Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215

UDI/DI (01) 0 5055196 96833 2, Lot 503150

Lot Numbers:
503150
Product: Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615

UDI/DI (01) 0 5055196 96834, Lot 503151

Lot Numbers:
503151

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 91183
Status: Active
Manufacturer: Corin Ltd
Manufactured In: United Kingdom
Units Affected: 2 products (5 units; 12 units)

Were You Affected by This Recall?

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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.