Class III — Low Risk

Low risk — use of or exposure to this product is not likely to cause adverse health consequences.

Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by Fresenius Medical Care Renal Therapies Group, LLC Due to Discolored powder has confirmed the presence of a...

Date: October 9, 2018
Company: Fresenius Medical Care Renal Therapies Group, LLC
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Fresenius Medical Care Renal Therapies Group, LLC directly.

Affected Products

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

Quantity: 92225

Why Was This Recalled?

Discolored powder has confirmed the presence of a foreign substance

Where Was This Sold?

This product was distributed nationwide across all 50 states.

Affected (51 states)Not affected

About Fresenius Medical Care Renal Therapies Group, LLC

Fresenius Medical Care Renal Therapies Group, LLC has 27 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report