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All product recalls associated with Clements Foods Co.
Total Recalls
1000
Past Year
898
Class I (Serious)
125
Most Recent
Jan 2026
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.
Ingredient (mustard seeds) tested positive for Salmonella
Potential for distal tip tearing of the Mechanical Lithotriptor V.
Defective container: Unable to get the solution out of the bottle as the spike of the cap was lodged in the nozzle of the product bottle
Complaints have been received regarding post-operative implant collapse.
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
This recall involves a decorative tree light controller that operates wirelessly to turn on holiday lights on a tree. The decorative controller contains two parts: a lever or a switch that can be pulled to turn the holiday lights on or off, and a separate white receiver that plugs into an outlet and into which the tree's holiday lights are plugged. The controller sold at Walmart and Cracker Barrel is shaped like a green, red and white peppermint candy with a candy cane on/off lever, and displays the words "Christmas Light Controller". The controller sold at Target is sold under the Wondershop™ brand and is shaped like a square on/off switch box with green, red and white balls, and displays the words "Tree Lighting Switch". The white wireless receptacle that is plugged into an outlet contains the words "Mr. Christmas" and one of these three model numbers printed on the white receptacle: 39611, 39612 or 39630.
Possible Salmonella contamination of affected product.
Incorrect labeling for seven manufactured lots of certain models of Arterial Cannulae.
Gas powered emergency resuscitator has a circuit flow controller manufactured with an undersized spring, which may cause resuscitator not reach the high and low ends of the PIP and PEEP pressure ranges, which may cause a loss of positive pressure, impacting effective ventilation of the patient.
False-positive MSI-H results generated by the Idylla MSI Test.
Oxygen concentrator may melt or catch on fire during use.
Product contains undeclared fish (anchovy) and soy.
There is a software issue that can result in the loss of patient monitoring on the Portrait Central Viewer Application after 425 days of continuous run-time.
Undeclared milk
Undeclared almonds
Undeclared wheat, Undeclared soybean oil
Undeclared milk
Undeclared milk
CGMP Deviations: presence of N-nitroso-duloxetine impurity above FDA recommended interim limit.