ICU Medical, Inc.

Frequent Recalls
16
Recalls
0
Units Recalled
0
Injuries
0
Deaths

Categories: Medical Device

2026-05-27 to 2026-09-23

DateSourceProductBrandSeverityUnits
2026-09-23FDA DeviceIV Sets with drip chambers Recall (Sep 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-09-23FDA DeviceIV Sets with drip chambers Recall (Sep 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-09-23FDA DeviceOncology sets with drip chambers Recall (Sep 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-09-23FDA DevicePlum administration sets Recall (Sep 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-09-23FDA DeviceIV Sets with drip chambers Recall (Sep 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-09-23FDA DeviceIV Non-Dedicated Gravity Administration Sets Recall (Sep 2026)ICU Medical, Inc.Class IIN/A
2026-09-23FDA DeviceIV Sets with drip chambers Recall (Sep 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-09-23FDA DeviceCADD Yellow Medication Cassette Reservoir Recall (Sep 2026)ICU Medical, Inc.Class IIN/A
2026-09-23FDA DeviceOncology sets with drip chambers Recall (Sep 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-07-29FDA DeviceHotline Fluid Warming Set Recall (Jul 2026) – ICU MedicalICU Medical Inc.Class IIN/A
2026-07-22FDA DeviceICU Medical Plum Solo Precision IV Pump Recall (Jul 2026)ICU Medical, Inc.Class IIN/A
2026-07-22FDA DeviceICU Medical Plum Duo Infusion Pump Recall (Jul 2026)ICU Medical, Inc.Class IIN/A
2026-06-17FDA DevicePlum Duo Precision IV Pump Recall (Jun 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-06-17FDA DevicePlum Solo Precision IV Pump Recall (Jun 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-06-17FDA DevicePlum Duo Infusion Pump Recall (Jun 2026) – ICU MedicalICU Medical, Inc.Class IIN/A
2026-05-27FDA DeviceOncology Kit w/60 Appx Recall (May 2026) – ICU MedicalICU Medical, Inc.Class IIN/A