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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.

December 22, 2021Medical DevicesFDA
Cardinal Health recalls SmartGown Breathable Surgical Gowns with raglan sleeves X-large, X-long, A-line SKU: 32474
Hazard: Potential for open packaging seals compromising the sterility of the surgical gowns
September 1, 2021Medical DevicesFDA
Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The proposed device is indic
Hazard: Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.
September 1, 2021Medical DevicesFDA
Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The proposed device is indi
Hazard: Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.
September 1, 2021Medical DevicesFDA
Cardinal Health recalls Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is ind
Hazard: Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls ACCU-CHEK SMARTVIEW 100 TEST STRIPS Item Number: 4742862
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls OPTICHAMBER DIAMOND SPACER WITH LARGE MASK Item Number: 4742326
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls ONETOUCH DELICA LANCETS 33G 100 COUNT Item Number: 5541628
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls ONETOUCH DELICA LANCETS 30G 100 COUNT Item Number: 5541610
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls ONETOUCH ULTRA TEST STRIPS 25 COUNT Item Number: 3510443
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls ONETOUCH ULTRASOFT LANCETS 100 COUNT Item Number: 3007788
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls ONETOUCH ULTRA BLUE TEST STRIPS 100 COUNT Item Number: 2990174
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls VAPORIZER VICKS 1.5GAL Item Number: 2354942
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls DEXCOM G6 SENSOR 3 PACK Item Number: 5447552
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls BD UF PEN 32GX4MM 100 NANO Item Number: 4292272
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls AEROCHAMBER PLS W/MASK LRG BLU Item Number: 1496033
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls FREESTYLE LIBRE 2 GLUCOSE MONITORING SYSTEM: Item number: 5658877
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls FREESTYLE LIBRE 14 DAY GLUCOSE MONITORING SYSTEM. Item Number: 5479084
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 30, 2021Medical DevicesFDA
Cardinal Health Inc. recalls FREESTYLE LANCETS 28G 100CT Item Number:2975670
Hazard: Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Enalapril Maleate Tablets, USP 2.5 mg 100 tablets Rx only Distributed by: Cardinal Health, NDC 64679-923-02
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Brompheniramine Maleate, Pseudoephedrine Hydrochloride and Dextromethorphan Hydrobromide Oral Syrup Net: 1 Pint (473 mL)
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls CYANOCOBAL Injection 1000MCG/ML 25X1ML; NDC/UPC 69680-112-25; RX; MULTI DOSE VIAL
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Corgard (nadolol tablets, USP) 40 mg 100 Tablets Rx only NDC 27505-101-01 Distributed by US WorldMeds, LLC, Louisville,
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls HALOPERIDOL TABLETS 20mg, USP, 100-count bottle, Rx Only Distributed by: Usher-Smith Laboratories, LLC, Maple Grove, MN
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Amantadine Hydrochloride Tablets 100 mg 100-count bottle, Rx Only Manufactured by Upsher-Smith Laboratories, Inc. Maple
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Briviact (brivaracetam) tablets 50 mg, 60-count bottle, Rx only Manufactured for UCB, Inc. Smyrna, GA 30080, NDC 50474-5
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls VIMPAT (lacosamide) Tablets, 200mg, 60-count bottle, Rx Only, Manufactured for: UCB, Inc. Smyrna, GA 30080, NDC 0131-24
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls VIMPAT(lacosamide) Tablets ,100 mg, 60-count bottle; Rx Only, Manufactured for: UCB, Inc. Smyrna, GA 30080
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls INTEGRA 325/40/3mg 90-count bottle, NDC: 52747-710-60
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls Restora Omega-3 enhanced Lactobacillus Casei KE-99 30 Capsules 1 A Day Nutritional Supplement NDC 52747-200-30 Marketed
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.
June 2, 2021DrugsFDA
Cardinal Health Inc. recalls TRAMADOL HYDROCHLORIDE TABLETS USP 100MG, 100-count bottle, Rx Only, Manufactured by: Rubicon Research :Private Limited,
Hazard: CGMP Deviations: Intermittent exposure to temperature excursion during storage.