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All product recalls associated with Beevers Manufacturing & Supply, Inc..
Total Recalls
4
Past Year
0
Class I (Serious)
0
Most Recent
May 2008
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.
Cannulaide recalled May 2008 due to improper seal of the pouch. The improper seal of the Cannulaide's package could potentially affect the device shelf life.
Cannulaide recalled May 2008 due to improper seal of the pouch. The improper seal of the Cannulaide's package could potentially affect the device shelf life.
Cannulaide model CA 101 was recalled because the firm discovered this model was packed and labeled as CA 102.