Fresh Recalls

Fresenius Medical Care Renal Therapies Group recalls

9 recent recalls on record for Fresenius Medical Care Renal Therapies Group in connected official government data as of October 22, 2026 at 6:00 PM UTC.

Models with recalls

5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3 (1)5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C (1)5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8 (1)5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 (1)Citrasate (1)CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors (1)Fresenius Medical Care (1)GRANUFLO Dry Acid Concentrate (1)NaturaLyte (1)

All Fresenius Medical Care Renal Therapies Group recalls

FDA Class II · Medical device · September 30, 2026

CombiSet Hemodialysis Blood Tubing Set with Attached Priming Set and Transducer Protectors recall — Fresenius Medical Care Renal Therapies Group, LLC

Communication to recommend reviewing the IFU and ensuring that all treatment preparation and handling steps are performed as instructed.

Official ID Z-3225-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

Citrasate recall — Fresenius Medical Care Renal Therapies Group, LLC

Complaints of blue-green discoloration in product

Official ID Z-3093-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

NaturaLyte recall — Fresenius Medical Care Renal Therapies Group, LLC

Complaints of blue-green discoloration in product

Official ID Z-3092-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

GRANUFLO Dry Acid Concentrate recall — Fresenius Medical Care Renal Therapies Group, LLC

Complaints of blue-green discoloration in product

Official ID Z-3091-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X HD/HDF with Twister Blood Tubing Set Part Number 03-5350-8 recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Official ID Z-3087-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X HD/HDF with CLiC Blood Tubing Set Part number 03-5300-3C recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Official ID Z-3086-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X HD/HDF Standard Blood Tubing Set Part Number 03-5300-3 recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Official ID Z-3085-2026 · Official record ↗

FDA Class II · Medical device · September 9, 2026

5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6 recall — Fresenius Medical Care Renal Therapies Group, LLC

Heightened probability of blood leak from the connection between the Arterial Alpha Clip and the main line or pump segment. Leak during treatment may lead to blood loss and hypovol…

Official ID Z-3084-2026 · Official record ↗

FDA Class II · Medical device · September 2, 2026

Fresenius Medical Care recall — Fresenius Medical Care Renal Therapies Group, LLC

Fresenius Medical Care Renal Therapies Group, LLC (FMCRTG) has received complaints regarding flow-, no water-, or temperature-related alarms with the 2008T¿ BlueStar Hemodialysis m…

Official ID Z-3017-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.