Cardinal Health Inc. Recalls Recalls by year
A bar chart of the number of recalls naming this company by year.
Recalls by year
Year Recalls 2021 86 2022 3 2023 6 2025 5
Download CSV FDA Recall
Terminated
Historical record Class II
POLYETHYLENE GLYCOL 3350 Powder for Solution Osmotic Laxative 14 once-daily doses 14 Packet- Newt Wt. 0.5 oz (17g) each NDC 45802-868-66 by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
HySept Solution 0.25% Sodium Hypochlorite Solution 473 mL (16 fl. oz.) NDC 39328-063-25 Manufactured in USA Patrin Pharma, Skokie, IL 60076 by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
Rybelsus (semaglutide) Tablets 7 mg Once daily Each tablet contains 7 mg semaglutide 30 tablets 3 blister packs. Each pack contains 10 tablets. Rx only NDC 0169-4307-13 Manufactured by: Novo Nordisk A/S DK-2880 Bagsvaerd, Denmark by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
CIPRODEX (CIPROFLOXACIN 0.3 AND DEXAMETHASONE 0.1%) 7.5ML; NDC/UPC 0078-0799-75; RX; DROPS by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
Ilevro (nepafenac ophthalmic suspension) 0.3% 3 mL Sterile Rx Only NDC 0065-1750-14 Alcon Laboratories, Inc. 6201 South Freeway Fort Worth, Texas 76134 by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
TOBREX 0.3% 3.5GM OPTH; NDC/UPC 65064435; RX; OINTMENT by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
Epinephrine Injection, USP Auto-Injectors in all strengths, packs and styles Manufactured for Mylan Specialty L.P., Morgantown, WV , NDC: 9502-500-01, 49502-500-02, 49502-500-92, 49502-501-01 by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
Estradiol Transdermal System, USP 0.1 mg/day (Twice-Weekly) Delivers 0.1 mg/day Rx only NDC 0378-4623-26 Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
Levothyroxine Sodium Tablets, USP 125 mcg (0.125 mg) 90 Tablets Rx only NDC 0378-1813-77 Mylan Pharmaceuticals Inc. Morgantown, WV 26505 U.S.A. by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
Belsomra (suvorexant) tablets 20 mg Each tablet contains 20 mg suvorexant. This package contains 30 Tablets in 3 Blister Cards. Each Blister Card contains 10 Tablets. Rx only NDC 0006-0335-30 Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. Whitehouse Station, NJ 08880, USA by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
PEDIA-LAX 66ML; NDC/UPC 301320202205; OTC; ENEMA by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
FDA Recall
Terminated
Historical record Class II
BENZOYL PEROXIDE WASH 5% 148ML; NDC/UPC 0536-1259-63; OTC; LIQUID by Cardinal Health Inc.
Reason
CGMP Deviations: Intermittent exposure to temperature excursion during storage. Published
June 2, 2021 Distribution
Multiple states
View recall →
This page lists recalls that name Cardinal Health Inc. as the recalling firm in the official source notice. It is
not a safety rating, ranking, or statement that the company acted negligently.
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