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All product recalls associated with Lovebiotics, LLC.
Total Recalls
1000
Past Year
303
Class I (Serious)
34
Most Recent
Nov 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.
Products listed sodium caseinate in allergen statement; however it did not further identify the allergen of milk.
This recall involves Bits and Pieces Fiber Optic indoor plug in Christmas tree. The full foliage branches have fiber optic light strands that change color. Each tree comes with an AC power adapter that is attached to the gold tone colored base that holds the tree in place. The AC power adapter plugs into a standard household outlet. The 18 inch tall tree item number is 43560 and weighs about three pounds. The 31 inch tall tree item number is 43559 and weighs about four pounds. The item numbers can be found on the UPC barcode label on the box.
Failed Content Uniformity Specifications
Cross Contamination With Other Products: metronidazole powder was found in one bottle of Divalproex Sodium.
Subpotent Drug
Subpotent Drug
Presence of particulate matter
Failed Stability Specifications
Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during routine stability testing.
Presence of Foreign Substance: Reports have been received of damaged StripPax packets containing silica gel desiccant potentially allowing the silica gel granules to make contact with Auryxia tablets in the bottle.
Microbial Contamination of Non-Sterile Products: potentially contamination with the bacteria Burkholderia cepacia
This recall involves all white plastic molded clip-on nocks used in arrows for Ravin brand crossbows. The white arrow nocks were sold separately in a package of 12 and as original equipment with Ravin crossbows and Ravin arrows. The white nocks measure about 0.9 inches long.
Labeling: Incorrect or Missing Lot and/or Exp Date - product label was missing lot number and beyond use date.
Failed Tablet/Capsule Specifications: confirmed customer complaint of thicker and heavier tablets in bottle.
Failed Impurities/Degradation Specifications: high out of specification test results obtained for individual and total impurities.
Failed Dissolution Specification
Presence of Foreign Tablets/Capsules: Risperidone Tablets were found in bottle of Paroxetine Tablets
Labeling: Incorrect Instructions. "TABLETS IN WEEK 4 ARE INACTIVE" printed on the blister foil and package insert, however,all tablets are active.
CGMP Deviations: Market complaints related to "gritty texture".
This recall involves all 2017 Arctic Cat Wildcat Trail SE (Special Edition) and Wildcat Sport SE ROVs with winch solenoids installed as original equipment and winch accessory kits sold separately for use on 2014 through 2017Arctic Cat Wildcat Sport and Wildcat Trail ROVs. The ROVs have four wheels, side-by-side seating for two people, and have a black chassis. "Wildcat Trail" or "Wildcat Sport" is printed on each side of the vehicle. In addition, Special Edition ROVs have "SE" printed on each side.