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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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Low RiskFDA Device

Fresenius Medical Care Renal Therapies Group, LLC: Discolored powder has confirmed the presence of a foreign substance

Agency Publication Date: November 29, 2018
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Affected Products

Product: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg 16.5 GAL Catalog Number: OFD2201-3B for hemodialysis

Lot code:18ETGF005

Lot Numbers:
code
Product: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg 16.5 GAL Catalog Number: OFD2251-3B for hemodialysis

Lot code: 18ETGF010 18HTGF002 18HTGF003 18HTGF007 18HTGF011 18HTGF013 18HTGF016 18JTGF005 18JTGF010 18JTGF012 18KTGF001 18KTGF011

Lot Numbers:
code
Product: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg 16.5 GAL Catalog Number: OFD3251-3B for hemodialysis

Lot code: 18BTGF016 18ETGF006 18ETGF014 18HTGF015 18LTGF003

Lot Numbers:
code

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 81451
Status: Resolved
Manufacturer: Fresenius Medical Care Renal Therapies Group, LLC
Manufactured In: United States
Units Affected: 3 products (4752; 92225; 22320)

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.