Official recall notice

FDA DeviceClass IINotable

FDA Recall: CADD Yellow Medication Cassette Reservoir with NRFit connector US Product Codes: 21-7600-24, 21-7

Recall date
2026-09-23
FDA class
Class II

Why it was recalled

Hazard

Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, exposure to infectious or toxic agents, or air embolus.

Product description

Reservoirs may exhibit medication leakage at the joint between luer connector and tubing. Issue could result in delay or interruption of therapy, under delivery of medication, exposure to infectious or toxic agents, or air embolus.

Affected products

21-7600-24 UDI-DI 30610586044001 Lots 6026878 6037784 6054015 6062724 6070616 6082332 6092886 6101906 6108556 6126029 6140893 6143454 6147696 6147697 6162769 6155095 6166032 6171587 6171586 21-7609-24 UDI-DI 30610586044018 Lot 6022079 6037697 6037698 6053978 6061525 6072970 6072964 6070575 6077773 6092846 6101798 6108514 6108515 6108516 6140862 6140861 6140865 6155132

Verify with the official notice →
Share:

Related Recalls

2026-09-23 · FDA_DEVICE
FDA Recall: Oncology sets with drip chambers
ICU Medical, Inc.
2026-09-23 · FDA_DEVICE
FDA Recall: IV Sets with drip chambers
ICU Medical, Inc.
2026-09-23 · FDA_DEVICE
FDA Recall: IV Non-Dedicated Gravity Administration Sets with drip chambers
ICU Medical, Inc.
2026-09-23 · FDA_DEVICE
FDA Recall: Oncology sets with drip chambers
ICU Medical, Inc.