Recall Z-3159-2026

ICU Medical, Inc. · initiated May 12, 2026

Open, Classified

Product

Oncology sets with drip chambers

Codes / lots: All products manufactured on or before 7/4/2026. UDI-DI: 10887709076768, 10887709088105

Reason for recall

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.

FDA-determined cause: Process control

Action taken

On 5/12/2026, the firm posted a Information Regarding Reported Black Specks in Certain IV Tubing Set Drip Chambers from ICU Medical document on their website. On 5/18/2026, updated the notices were sent. On 7/28/2026, correction notices were sent to customers asking them to do the following: 1) Share this notification with all potential users of the device to ensure they are aware of this notification. If the devices are used or further distributed to another location, please ensure that this communication is delivered there. 2) Complete and return the attached Customer Response Form to MarketAction@mailac.custhelp.com 3) Continue using products as intended and per facility protocol. 4) Report any product quality concerns to ICU Medical Complaint Management. Firm contacts: GlobalComplaints@icumed.com 1-866-261-8806. customerservice@icumed.com 1-800-258-5361

Details

Recall number
Z-3159-2026
Initiated
May 12, 2026
Posted by FDA
September 11, 2026
Product code
ONB – Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System
Quantity
28,550
Distribution
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.
Recalling firm
ICU Medical, Inc., San Clemente, CA

Official FDA recall record

Other products in the same recall event

RecallProductInitiated
Z-3156-2026 Plum administration setsIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic… 05/12/2026Open, Classified
Z-3157-2026 IV Non-Dedicated Gravity Administration Sets with drip chambersIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic… 05/12/2026Open, Classified
Z-3158-2026 Oncology sets with drip chambersIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic… 05/12/2026Open, Classified
Z-3160-2026 IV Sets with drip chambersIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic… 05/12/2026Open, Classified
Z-3161-2026 IV Sets with drip chambersIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic… 05/12/2026Open, Classified
Z-3162-2026 IV Sets with drip chambersIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic… 05/12/2026Open, Classified
Z-3163-2026 IV Sets with drip chambersIntravascular administration tubing set drip chambers may have black specks potentially due to the plastic… 05/12/2026Open, Classified