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All product recalls associated with Medical Action Industries, Inc..
Total Recalls
18
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2024
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.
The protective pouches were identified to have been improperly labeled with UDI that is associated with an incorrect GMDN (Global Medical Device Nomenclature) code. These blue foam pouches were misused due to misclassification of the GMDN.
The kits contain saline flush syringes which were recalled by the supplier.
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