medical MODERATE Updated 2026-09-23

ICU Medical, Inc. recalls IV Sets with drip chambers

See all recalls from ICU Medical, Inc. →

Recalled Product

IV Sets with drip chambers

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Hazard / Issue

Intravascular administration tubing set drip chambers may have black specks potentially due to the plastic molding process leaving discolored polyvinyl chloride (PVC) material within the drip chamber wall. The presence of discoloration and particulate matter in the fluid path has not been ruled out.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: All products manufactured on or before 7/4/2026. UDI-DI: 20887787005831

✅ 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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