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All product recalls associated with Cardinal Health.
Total Recalls
1000
Past Year
631
Class I (Serious)
65
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.
Counterfeit mesh product labeled as Ethicon Prolene Polypropylene Mesh, product code PMII.
The manufacturer's instructions for using radiation treatment software may cause healthcare practitioner to mistreat the patient.
Use of the dialyzers may cause iritis (red-eye) patient reactions.
The walk-behind lawn mowers are gas-powered and have an orange body with a black push-handle. They are capable of being operated with or without a bag attachment. The model number and serial number can be found on a decal mounted above the left rear wheel axle.
Datex-Ohmeda Cardiocap/5 Patient Monitors have bracket pins which do not adequately secure them to their optional mounting stand so the monitors may fall.
Heater vent door on neonatal incubator may malfunction.
The paperback book is titled "Candle & Soap Making For Dummies." The book's cover is black and yellow and has a photograph of candlesticks and slices of soap.
Hardware of the camera coupler may rust and result in an ineffective sterilization/cleaning process.
The saline bags may inappropriately empty/fill during the recirculation mode of the hemodialysis system.
This recall involves all Segway HT i167 ("i Series") models sold to consumers. In addition, Segway LLC is including all e167 ("e Series") and i167 models sold to commercial users, and all p133 ("p Series") models sold to consumers in test markets.
Software Defect. When orders are modified before the Roche Cobas Integra query for a specimen, the sample ID locks.
The recalled Home Line bunk beds include the following models and styles: S130 (black), S131 (white), S132 (red), and S133 (blue) have a single top mattress and a double width bottom mattress; S135 (black) and S136 (white) that have a single top and a single bottom mattress; and S116 (black) and S117 (white) that have a single top mattress and a bottom mattress that also converts into a couch. Some units are labeled with the "Home Line" name and the model numbers on the top front railing.
The recall includes all Hayward H-Series ED2 natural-draft pool heaters with model numbers: H150ED2 H250PED2 H350PED2 H150PED2 H250PEDH2 H400ED2 H200ED2 H300ED2 H400PED2 H200PED2 H300PED2 H250ED2 H3503D2 A manufacturing label displaying the unit's model number and serial number is inside the unit, on the heater floor. Consumers can access the label by removing the front panel of the heater housing. The H-series ED2 Control Bezel assembly (a black box mounted behind the front control panel) encases the defective circuit board.
Wright Medical commercially distributed Transcend alumina acetabular shell liners lacking the required process validation.
Software defect. Clinical Laboratory results failing quality assurance were filed directly to a patient's chart without review.
Under specific sequence conditions, the unit may apper to be infusing, but is not
The Happyvillagers are made with birchwood and painted with various villager images. The sets were sold separately with 12 villagers per set and as a part of the Happyville Special set that included a set of 35 Happyville Blocks. Only the Happyvillagers are included in the recall.
Software Design Defect. Under certain conditions, results are removed.
Software Defect. Data used in the diagnosis and or treatment of a patient's illness are missing from the patient result report.
Software design deficiency. If the dilution factor is added to the same result twice, incorrect specimen values are reported.