medical MODERATE Updated 2026-09-09

Fresenius Medical Care Renal Therapies Group, LLC recalls 5008X Standard HD Pre-Flush Standard Blood Tubing Set

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Recalled Product

5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6

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Hazard / Issue

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 hypovolemia.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lots 25KR01227 25NR01257 UDI-DI 00840861102556

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.

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Search Amazon for 5008X Standard HD Pre-Flush →

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