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All product recalls associated with Action Products Incorporated.
Total Recalls
2
Past Year
0
Class I (Serious)
0
Most Recent
Jun 2009
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.
Medical device intended for use by healthcare practitioners was incorrectly labeled. 1.0 cm thick pad was labeled as 0.5 cm thickness, and vice versa.
Wheelchair seat may not properly support the user due to cracks in the plastic seat base.