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All product recalls associated with Cardinal Health 203, Inc.
Total Recalls
492
Past Year
16
Class I (Serious)
7
Most Recent
Nov 2025
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.
Ventilators have not consistently switched to internal battery operation when the external DC power source has become inadequate to supply stable power. This situation results in loss of ventilation to the patient.
The products labeled as sterile are not sterile.
The products labeled as sterile are not sterile.
The product was not held at the labeled storage temperatures, which could affect the product potency and/or physical properties, were distributed.