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All product recalls associated with Cardinal Health.
Total Recalls
1000
Past Year
592
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.
A small piece of the stylet sheath has the potential to shear off upon removal of the stylet from the tracheal tube.
Lack of Assurance of Sterility: Complaints of leaks due to an incomplete seal at the bag seam.
Product may be contaminated with Listeria monocytogenes
Out-of-specification result for pH observed during stability testing of Ferrous Sulfate Elixir, 5 mL unit dose, Lot 621120.
This recall involves vinyl polystyrene-filled bean bag chairs with a single zipper on the exterior cover. The round vinyl bean bag chairs measure 88 and 98 inches in diameter. Colors and patterns included in the recall are black, hot pink, lime, purple, royal blue, ruby red, and baseball, basketball, football and soccer ball. A tag sewn into bean bag chair's cover seam reads "Made By Comfort Research" and "100% Polystyrene."
An issue was identified with the mAs accuracy check performed on the system that could result in inaccuracies in the 10% to 20% range for exposure times longer than 15 msec.
Potential safety issue due to a required torque check on three bolted joints of the Revolution CT scanner. No injuries or illnesses reported.
An issue was identified with the mAs accuracy check performed on the system that could result in inaccuracies in the 10% to 20% range for exposure times longer than 15 msec.
An issue was identified with the mAs accuracy check performed on the system that could result in inaccuracies in the 10% to 20% range for exposure times longer than 15 msec.
Transmitter may initiate a software reset resulting in backup operation in some implanted St. Jude Medical Radio Frequency (RF) enabled Implantable Cardioverter Assura, Unify Assura, and Quadra Assura ICDs and Assurity and Allure Pacemakers.
Microbial Contamination of Non Sterile Product; microbial assay reported unacceptable high plate counts and positive for E. Coli
Control units were equipped with an internal mounting kit that does not meet medical safety standards, and are conductive, increasing the risk of electric shock to the user and patient. These units were manufactured prior to Pivotal Health Solutions acquisition of the Apollo product line.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.
FDA samples found the presence of Listeria Monocytogenes in three varieties of cheese.