Drug recall

Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Non-vented stopper included…

FDA recall event 97317 · Class II · ICU Medical Inc.

Key facts

Event ID 97317
Recall numbers Z-2522-2025, Z-2523-2025, Z-2524-2025, Z-2525-2025, Z-2526-2025, Z-2527-2025
Recalling firm ICU Medical Inc.
Product type Devices
Products Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Non-vented stopper included. 100mL, Product Code 21-7002-24, Smiths Medical CADD Medication Cassette Reservoir with clamp and female Luer. Nonvented stopper included. 50mL, Product Code 21-7001-24, Smiths Medical CADD Medication Cassette Reservoir with flow stop, clamp and female Luer. Non-vented stopper included. 100mL, Product Code 21-7302-24, Smiths Medical CADD" Medication Cassette Reservoir with flow stop, clamp and female Luer. Non-vented stopper included. 50mL, Product Code 21-7301-24, Smiths Medical CADD" Yellow Medication Cassette Reservoir with flow stop, clamp and female Luer. Non-vented stopper included 100mL, Product Code 21-7300-24 and 1 more
Classification Class II
Status Ongoing
Voluntary or mandated Firm Initiated
Reason for recall Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along…
Initiation date Aug 6, 2025
Report date Sep 10, 2025
City Minneapolis
State MN
Country United States
FEI number 3012307300

At a glance

  • 1–9 Products in this recall
  • 1–9 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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