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ICU Medical Z0750Recalls & reported problems

Icu Medical, Inc. · 138" (351 cm) 20 Drop Y-Type Blood Set, 200 Micron Filter, 2 Clave®, Pre-Pierced Port, 4-Way Stopcock, Rotating Luer · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
0
Deaths reported
0
Injuries reported
0
Recalls naming it
1

Summary

No MAUDE adverse event reports in our data reference this device identifier directly.

1 FDA recall record name this device's identifier, 1 still open.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Recalls naming this device

  1. May 12, 2026Class IIOpen, Classified

    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.

    Z-3163-2026 · Root cause: Process control · Recall details · FDA record ↗

Other SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE devices

All SET, TUBING, BLOOD, WITH AND WITHOUT ANTI-REGURGITATION VALVE devices →

Sources and updates

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