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All product recalls associated with MERCEDES-BENZ.
Total Recalls
1000
Past Year
434
Class I (Serious)
138
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.
MERCEDES-BENZ IS RECALLING CERTAIN MODEL YEAR 2007-2009 E350 4MATIC WAGON VEHICLES MANUFACTURED FROM JULY 1, 2006, THROUGH APRIL 30, 2009. A CONNECTING ROD FOR THE LOAD LEVELING REAR SUSPENSION SYSTEM MAY FAIL.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flavours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its subsidiary STP Specialty Foods, Inc. because the recalled products contained a seasoning blend manufactured by Kerry with lactic acid which may contain small metal fragments.
NAVISTAR IS RECALLING CERTAIN MODEL YEAR 2007, 2009, AND 2011 IC CESB SCHOOL BUSES EQUIPPED WITH BRAUN CENTURY-2 AND VISTA-2 WHEELCHAIR LIFTS. OVER TIME, AND WITH FREQUENT USE, THE ROLL STOP LATCHES ON THE OUTER BARRIER MAY BECOME BENT OR MISALIGNED.
The product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Product ("Digestive 3 in 1 Health") was manufactured using a raw ingredient that tested positive for Salmonella by the raw ingredient supplier.
Korean Oysters are recalled because the products have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
This recall involves eight models of Happy Mouth wire mouth bits used with a bridle in horseback riding. The bits involved in this recall have steel braided wire running through the plastic mouthpiece and most with a metal ring on each end. Model numbers included in the recall are 462172SS, 462177SS, 462181SS, 462184SS, 464123SS, 466898SS, 466904SS and 467248SS. Model numbers can be found on a label attached to the product. "Happy Mouth" is engraved on the plastic mouthpiece.
Chicken of the Sea is recalling Oysters supplied by Chicken of the Sea under the Chicken of the Sea, Pacific Pearl, and Ace of Diamonds brands because the products have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Chicken of the Sea is recalling Oysters supplied by Chicken of the Sea under the Chicken of the Sea, Pacific Pearl, and Ace of Diamonds brands because the products have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Chicken of the Sea is recalling Oysters supplied by Chicken of the Sea under the Chicken of the Sea, Pacific Pearl, and Ace of Diamonds brands because the products have been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or whereby it may have been rendered injurious to health.
Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.
Lack of Assurance of Sterility: Franck's Lab Inc. initiated a recall of all Sterile Human Drugs distributed between 11/21/2011 and 05/21/2012 because FDA environmental sampling revealed the presence of microorganisms and fungal growth in the clean room where sterile products were prepared.