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All product recalls associated with ADAC Laboratories.
Total Recalls
1000
Past Year
100
Class I (Serious)
84
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.
A software defect, relating to the motorized wedge functionality when using an Elekta linear accelerator, can result in incorrect dose delivery to the patient. Also, dose delivery in the wrong location may occur when using a Elekta Leksell headframe.
Dose delivery in the wrong location may occur when using a Elekta Leksell headframe.
The balloons may be defective as indicated by an increased number of early balloon failures, which may result in tube displacement from patient.
Incorrect Test Results-product may show a higher than expected platelet background count when used on the CELL-DYN 4000 System and report patient results that are unacceptable (out-of-range).
The package inserts contain incorrect control values for the urinary free cortisol extraction procedure.
The recalled candles were sold in packages containing eight tea light candles and one glass holder in the shape of a flower. The 1-inch-tall candles were available in either gold or silver. A label affixed to the top of the package containing the recalled candles reads "Luminessence™ candles, 8 T-Lite Candles with Glass Holder, NET WT 3.2 oz (EACH 10G)." The label affixed to the bottom of the package reads, "DOLLAR TREE DIST., CHESAPEAKE, VA 23320, MADE IN CHINA."
Potential loose header (end cap) on hollow fiber dialyzers.
Potential loose header (end cap) on hollow fiber dialyzers.
Complaints that instructions for use were not clear.
18 gauge needles in Central Venous Catheter kits may be partially occluded.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
Device was distributed without the dome part accessory, part number 350-DOMPK
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.
The is an increase in the number of control values out of range low, and diluted patient specimens may yield lower than expected results.