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All product recalls associated with GE PHARMA LLC -.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
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.
Product contains 1,3 dimethylamylamine (DMAA)
OIKOS Nonfat Yogurt Blueberry Flavor Single Serve 5.3 oz cups were recalled because the lid correctly identifies the product but the cup is incorrectly labeled as blackberry flavor. Additionally, the product is blueberry flavored but the ingredient statement is for the blackberry flavor, which does not declare carmine, a potential allergen ingredient that is used in manufacturing the blueberry fla
Inadequate pasteurization
Inadequate pasteurization
Presence of Particulate Matter; Glass particulates observed in vials
Incorrect/ Undeclared Excipients: NyQuil Liquid Original bottles were inadvertently overwrapped with NyQuil Liquid Cherry information as a result the outer wrap does not correctly identify color additives, particularly FD&C Yellow No. 6 and FD&C Yellow 10.
Inadequate pasteurization
The recall involves Vitamix 64-ounce Low-Profile containers with blade part number 103208 A and blade date codes 03-12 (March 2012) through 07-13 (July 2013). The blade part number and date code are laser etched onto the top of the blade at the bottom of the container. The clear, plastic, 64-ounce container with black plastic handle and lid was sold with Vitamix blender models 7500, Professional Series 300, Professional Series 750 and individually. Replacement blades with part number 104602 A are not affected.
Bombardier Recreational Products (BRP) is recalling certain model year 2013 Can-Am Spyder RT series and ST series motorcycles. The tandem brake master cylinder manifold inlet may melt allowing the brake fluid to leak out.
Coliform level exceeds product specification
Finished product labels declared butter or cream but milk is not listed.
Finished product labels declared butter or cream but milk is not listed.
Finished product labels declared butter or cream but milk is not listed.
Finished product labels declared butter or cream but milk is not listed.
Undeclared whey powder (milk allergen) sub-ingredient of chocolate confectionery coating used in manufacturing of Black & White Cookies.
Bubbles Baking Co. is recalling coffee cake muffins because it may contain undeclared pecan nuts.
Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS results were reported to customers as passing. Hence the sterility of these products cannot be assured.
Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS results were reported to customers as passing. Hence the sterility of these products cannot be assured.
Lack of Assurance of Sterility: Pharmacy Creations is recalling Lidocaine 1% PF Sterile Injection and EDTA disodium 150 mg/mL due to lack of assurance of sterility.
Lack of Assurance of Sterility: Leiter Pharmacy is recalling due bacterial contamination found after investigation at contract testing laboratory discovered that OOS/failed results were reported to customers as passing. Hence the sterility of these products cannot be assured.