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All product recalls associated with McKesson General Medical Corporation.
Total Recalls
1000
Past Year
1000
Class I (Serious)
34
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 product is an unapproved medical device with associated potential health hazard.
Surgical devices intended for single use were not labeled for single use.
Mislabeled with wrong drop size drip chamber specification.
Under certain conditions the tilt mechanism of the strollers may not function properly allowing the child to fall out if the seat belt is not fastened.