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Cardinal Health Inc.

Cardinal Health Inc. Recalls

All product recalls associated with Cardinal Health Inc..

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Recall Summary

Total Recalls

1000

Past Year

593

Class I (Serious)

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 1341–1360 of 10391 recalls

Lubricant Eye Drops (Leader) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• Cardinal Health Inc.

Lubricating Eye Drops (Major) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Lubricant Eye Drops (Leader) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

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Class IHigh

FDAOct 31, 2023Nationwide• Cardinal Health Inc.

Eye Irritation Relief (Leader) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• Cardinal Health Inc.

Dry Eye Relief (Leader) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• Cardinal Health Inc.

Lubricant Eye Drops (Leader) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• Cardinal Health Inc.

Lubricating Tears Eye Drops (Major) – non-sterile manufacturing (2023)

Non-Sterility: FDA found insanitary conditions and positive bacterial test results from environmental sampling at the manufacturing facility.

Class IHigh

FDAOct 31, 2023Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Lisinopril Tablets 20mg (NCS) – foreign tablets risk (2023)

Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots

Class IIILow

FDAOct 27, 2023Nationwide• NCS Healthcare of Kentucky Inc

Buspirone Hydrochloride Tablets 10mg (NCS) – foreign tablets risk (2023)

Presence of Foreign Tablets: Potential of stray tablet(s) of Amlodipine Besylate 10 mg Tablet within the recalled lots

Class IIILow

FDAOct 27, 2023Nationwide• NCS Healthcare of Kentucky Inc

RAPIDPoint Cartridge (Siemens) – sodium sensor bias (2023)

RAPIDPoint 500 Systems Measurement Cartridges (with lactate) has the potential to affect the Sodium (Na+) sensor to produce a negative bias that could result in serious injury due to a delayed diagnosis of hypernatremia or unnecessary intervention for hyponatremia and result in iatrogenic hypernatremia especially if the true sodium result is near the thresholds of severe alterations, as well as cause a Question Result -----? error flag for multiple electrolytes on patient samples and quality control that may cause a delay of diagnosis or treatment.

FDAOct 26, 2023Nationwide• Siemens Healthcare Diagnostics Inc

Bobcat Zero-Turn Lawnmowers – crash risk (2023)

Laceration Risk

This recall involves Bobcat-branded and Kubota-branded stand-on zero-turn lawnmowers. The Bobcat stand-on zero-turn lawnmowers are black and white with the Bobcat name and logo on an orange background. They also have orange wheel wells. The Kubota stand-on zero-turn lawnmowers are orange and black with the Kubota name in white and orange wheel wells. The following model and serial numbers, located on the right side of the frame just above the operator platform, are included in this recall. The recalled engines are model year 2023 FR730V, FR691V, and FR651V. The recalled engine model and serial numbers are located on the engine fan housing. The following model and serial number ranges are included in this recall. Bobcat: MODEL SERIAL NUMBER ZS4036 999400100961 thru 999400100973 999400100975 thru 999400101046 999400101049 thru 999400101053 999400101055 ZS4036 SJAU 9994001AU80157 thru 9994001AU80165 9994001AU80168 thru 9994001AU80169 ZS4048 999400201096 thru 999400201170 ZS4048 SFAU 9994002AU00141 thru 9994002AU00145 ZS4052 999400301247 thru 999400301380 999400301382 thru 999400301385 999400301387 thru 999400301397 ZS4052 SKAU 9994003AU00125 ZS4061 999400400750 thru 999400400822 999400400826 thru 999400400831 999400400833 thru 999400400834 999400400836 thru 999400400838 ZS4061 SKAU 9994004AU00111 thru 9994004AU00112 Kubota: MODEL SERIAL NUMBER SZ19NC-36-2 14490 thru 14517 14618 thru 14620 14678 thru 14679 14803 thru 14818 14835 thru 14850 14856 thru 14857 14922 thru 14927 15051 thru 15062 SZ22NC-48-2 14380 14401 thru 14412 14566 thru 14568 14666 thru 14677 14695 thru 14700 14706 thru 14711 14790 thru 14796 14858 thru 14869 14928 thru 14931 15030 thru 15044 SZ26NC-52-2 14429 thru 14446 14466 thru 14471 14474 14484 thru 14489 14577 thru 14609 14692 thru 14694 14701 thru 14705 14712 thru 14717 14780 thru 14783 14872 thru 14888 14892 14921 14944 thru 14967 14992 thru 15007 SZ26NC-61-2 14417 thru 14425 14475 thru 14483 14622 thru 14643 14718 14763 thru 14771 14893 thru 14904 14971 thru 14991 15014 thru 15026 SZ19-36-2CAD 14558 thru 14565, 14801 SZ22-48-2CAD 14569 thru 14576, 14870 thru 14871, 15045 SZ26-61-2CAD 15009 thru 15013, 15029 1698562

CPSCOct 26, 2023Nationwide• Doosan Bobcat North America, of West Fargo, North Dakota

INDICAID COVID-19 Test (Phase Scientific) – incorrect expiration (2023)

COVID-19 rapid antigen at home tests were released with an incorrect expiration date of 05 April 2024 when the correct expiration should be 21 February 2024. Expired tests could produce invalid or inaccurate results.

FDAOct 25, 2023Nationwide• PHASE SCIENTIFIC INTERNATIONAL LIMITED 1/f, E Phase 3 Hong Kong Science Park Sha Tin Hong Kong SAR

SmartPath dStream 1.5T (Philips) – fire potential (2023)

Fire/Burn Risk

Potential component failure in the Gradient Coil could product smoke and/or fire.

FDAOct 23, 2023Nationwide• Philips North America Llc

Achieva 1.5T (Philips) – fire potential (2023)

Fire/Burn Risk

Potential component failure in the Gradient Coil could product smoke and/or fire.

FDAOct 23, 2023Nationwide• Philips North America Llc

Achieva 1.5T Initial System (Philips) – fire potential (2023)

Fire/Burn Risk

Potential component failure in the Gradient Coil could product smoke and/or fire.

FDAOct 23, 2023Nationwide• Philips North America Llc

Intera 1.5T Power/Pulsar (Philips) – fire potential (2023)

Fire/Burn Risk

Potential component failure in the Gradient Coil could product smoke and/or fire.

FDAOct 23, 2023Nationwide• Philips North America Llc

Ingenia 1.5T CX (Philips) – fire potential (2023)

Fire/Burn Risk

Potential component failure in the Gradient Coil could product smoke and/or fire.

FDAOct 23, 2023Nationwide• Philips North America Llc

Achieva 1.5T Conversion (Philips) – fire potential (2023)

Fire/Burn Risk

Potential component failure in the Gradient Coil could product smoke and/or fire.

FDAOct 23, 2023Nationwide• Philips North America Llc

Phenytoin Oral Suspension (Major) – content uniformity issue (2023)

Failed Content Uniformity Specifications

Class IHigh

FDAOct 23, 2023Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Intera 1.5T (Philips) – fire potential (2023)

Fire/Burn Risk

Potential component failure in the Gradient Coil could product smoke and/or fire.

FDAOct 23, 2023Nationwide• Philips North America Llc