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All product recalls associated with Solace International Inc.
Total Recalls
1000
Past Year
135
Class I (Serious)
159
Most Recent
Dec 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.
Labeling: Labeling Bears Unapproved Claims; Dermatend is not FDA approved and therefore has not been shown to be safe and effective for the uses suggested in the labeling.
The component supplier recalled their 0.9% Sodium Chloride Injection USP BD Posiflush SF Saline Flush Syringe 10mL because some unit packages may exhibit open seals which impact package integrity and potentially product sterility.
This recall involves bar stools with a dark brown walnut finish wood with a brown leather padded back and swivel seat cushion. The stools have four legs with a footrest connecting each leg and measure 21 inches wide, 48 inches high and 23 inches deep. This recall includes stools with Samson item number M3216604 and Customer item number 845275 found on the bottom of the seat cushion.