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Cardinal Health Recalls
316 recalls on record · January 30, 2013 to September 3, 2025 · Drugs, Food & Beverage, Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Synthroid (levothyroxine sodium tablets, USP) in all pack sizes, styles and concentrations Rx only Abbott Laboratories N
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Norvir Ritonavir Tablets 100 mg 30 Tablets Rx only NDC 0074-3333-30 Abbott Laboratories North Chicago, IL 60064, U.S.A.
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Orilissa elagolix tablets 150 mg per tablet equivalent to 155.2 mg elagolix sodium, 28 Tablets For 28 Days Rx only NDC 0
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Creon (pancrelipase) Delayed-Release Capsules Dose By Lipase Units Lipase 36,000 USP Units Rx only NDC 0032-3016-13 100
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls NIACIN 250MG 110; NDC/UPC 740985228494; OTC; TABLETS
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls THERAPEUTIC M 130; NDC/UPC 740985223680; OTC; TABLETS
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
April 7, 2021DrugsFDA
Cardinal Health Inc. recalls Tremfya (guselkumab) Injection, 100 mg/mL, one single-dose prefilled syringe per carton, Rx only, Manufactured by: Janss
Hazard: Temperature Abuse
June 3, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Kangaroo 924 Safety Screw Spike Set, Product Code 775759
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
June 3, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Kangaroo Epump Safety Screw Spike Set, Anti-free Flow, Product Code 775659
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
June 3, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Kangaroo Epump Safety Screw Spike with Flush Bag, Anti-free Flow, 1000 mL, Product Code 775100
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
June 3, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Kangaroo Connect ENPlus Spike Set Anti-free Flow, Product Code 77000FD
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
June 3, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Kangaroo Joey Safety Screw Spike Set, Anti-free Flow, Product Code 765559
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
June 3, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Kangaroo Joey Safety Screw Spike with Flush Bag, Anti-free Flow,1000 mL, Product Code 765100
Hazard: The feeding spike sets may leak at the interface of the tube and spike connector.
May 27, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Strep B Carrot Broth One-Step, 16x100mm Tube, 6ml, Item code Z46BX - Product Usage: Intended to detect Group B Streptoco
Hazard: Three products requiring refrigerated storage conditions were incorrectly stored outside of approved temperature ranges. Using these temperature abused products may result in misdiagnosis of the patient.
May 27, 2020Medical DevicesFDA
Cardinal Health Inc. recalls Professional Urine Drug Control, Item code 88010 - Product Usage: The Alere Professional Cup Urine Drug Controls are com
Hazard: Three products requiring refrigerated storage conditions were incorrectly stored outside of approved temperature ranges. Using these temperature abused products may result in misdiagnosis of the patient.
May 27, 2020Medical DevicesFDA
Cardinal Health Inc. recalls B-Hydroxybutyrate LiquiColor, Item code CH2440058 - Product Usage: Product is used for the quantitative determination of
Hazard: Three products requiring refrigerated storage conditions were incorrectly stored outside of approved temperature ranges. Using these temperature abused products may result in misdiagnosis of the patient.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 FABREINF SURG GOWN LARGE, Item Code 9511
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NONREINF SURGICAL GOWN 3XL, Item Code 9585
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NON-REINF SURG GWN XL 2 TWL, Gown Item Code ASG9545
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NON-REINF SURG GOWN LG 2 TWL, Item Code ASG9515
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 FABRNF SURGGWN XL LONG 2 TWL, Gown. Item Code ASG9541EL
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 FABRNF SURG GWN XL 2 TOWELS, Gown. Item Code ASG9541
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 FABRNF SURG GOWN L 2 TOWELS, Item Code ASG9511
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NON-REINF SURGICAL GOWN XL, Item Code 9545
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls GOWN SURG LG W/TOWEL ST BACK, Item Code 9515
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NON-REINF SURG GWN 3XL XLONG, Gown. Item Code 95995
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NONREINF SURGICAL GOWN 4XL, Item Code 9599
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NONREINF SURG GOWN 2XL XLONG, Item Code 9575EL
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls AAMI 3 NON-REINF SURGICAL GOWN XXL, Item Code 9575
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.
February 12, 2020Medical DevicesFDA
Cardinal Health recalls ROYALSILK XLARGE, Gown. Item Code 9548
Hazard: The gowns contain an unknown level of bioburden, unknown microbiological flora, and unknown particulate contamination.