FDA-Device2026-09-23Class IIPROCESSING DEFECT

ICU Medical oncology IV tubing sets recalled for black specks in drip chambers

OTHERNationwide distributionMedical devices

What this means

ICU Medical oncology IV tubing sets may contain small black specks in the drip chamber. These specks are discolored plastic from the manufacturing process and do not enter the fluid path. Healthcare providers who notice them may replace the tubing set before use, which could delay patient treatment.

  • Check oncology IV tubing sets for black specks in the drip chamber before use.
  • If you see black specks, do not discard the set automatically — contact ICU Medical or your healthcare facility for guidance.
  • Contact ICU Medical or your hospital's medical device safety team if you have questions about affected products.
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The agency's original wording
Hazard

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 that does not enter the fluid path, which if seen by a healthcare provider may lead to replacement of product before use, which could result in a delay in therapy.

Intended for
Adults
Illnesses reported
None reported
Sold states
Worldwide - US Nationwide distribution including in the states and territories of ND, TX, CT, KY, CO, AR, NC, NJ, VA, MD, OK, AK, IA, IN, KS, OR, CA, OH, WA, GA, AL, SC, MA, HI, FL, NH, NE, MN, MS, SD, MT, NY, DC, ID, WI, PA, AZ, MO, NV, TN, NM, WV, WY, IL, UT, MI, RI, VT, LA, DE, ME, VI, GU, PR and the countries of PK, PH, MY, HK, IN, DE, CR.
Affected count
28,550
Manufactured in
951 Calle Amanecer, N/A, San Clemente, CA, United States
Products
Oncology sets with drip chambers

Official notice

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3159-2026

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