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All product recalls associated with MERCEDES BENZ.
Total Recalls
1000
Past Year
432
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 USA, LLC (MBUSA) is recalling certain 2006-2007 C350, C230, C280, CLK350, E320CDI, E350 Wagon, E350, 2006 C55 AMG, CLK500, CLS500, CLS55 AMG, E500 Wagon, E500, E55 AMG, 2007 CLK550, CLS550, CLS63 AMG, E550, E63 AMG, and E63 Wagon AMG vehicles. The bonding between the glass panel and the sliding roof frame may deteriorate, possibly causing the glass panel to detach from the vehicle.
Labeling: Illegible label: Manufacturer received complaint of mis-alignment print of the printed dosing instructions on the blister card.
This recall involves bottles of the prescription drug Evrysdi, a prescription medicine used to treat spinal muscular atrophy (SMA) in adults and children 2 months of age and older. The recalled 100 mL amber bottles have "Evrysdi (risdiplam) for oral solution," the dosage and "NDC 20242-175-07" on the front of the bottle labels.
Discrepancy in labeling between the adult CBC reference ranges presented in the OLO Operator's Manual and the OLO software
Positive Control may run high out of its assigned ISR range and result in an invalid run and necessitate retesting
This recall involves Lifetime Products 6-Foot Seminar Tables with model #80176. The tables have gray metal frames and white plastic tops. The tables measure 6 feet long by 18 inches wide by 28 inches high. The "Lifetime" logo is molded into each end of the upper surface of the table top. A green product ID sticker located on the underside of the table has the model number and the year and chronological day of manufacture in the first five digits (Example: June 23, 2020 = 20175), followed by a two-digit number for the factory. The recalled tables were manufactured between August 7, 2016 (16220) and June 23, 2020 (20175).
Daimler Vans USA, LLC (DVUSA) is recalling certain 2019-2020 Mercedes Benz Sprinter vehicles equipped with an optional electric sliding door. The auxiliary lock on the sliding door may be the incorrect type for an electric sliding door. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 226, "Ejection Mitigation."
CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.
Microbial Contamination of Non-Sterile Products: firm's internal testing found certain lots of the product to be contaminated with Burkholderia contaminans and/or yeast and mold.
CGMP Deviations: lots recalled due to CGMP deviations because they were manufactured under the same conditions as product lots found to be contaminated.
Microbial Contamination of Non-Sterile Products: firm's internal testing found certain lots of the product to be contaminated with Burkholderia contaminans and/or yeast and mold.
Combi USA, Inc. (Combi) is recalling certain Combi BabyRide Infant Car Seats, model 378099 with dates of manufacture of 5/1/2016 thru 8/31/2019. The 1-inch-wide webbing strap used in the center front adjuster to adjust the shoulder harness straps fail the minimum initial breaking strength requirements, and in certain circumstances, may not adequately restrain a child during a crash. As such, these car seats fail to conform to Federal Motor Vehicle Safety Standard (FMVSS) number 213, "Child Restraint Systems."
Custom Truck And Body Works (Custom Truck) is recalling one 2016 Ford F550 vehicle and one 2018 International 4000 vehicle equipped with 7x9 combination LED Stop-Tail-Turn reverse lights. The lights may be too bright, exceeding the maximum light output allowed which may adversely affect the vision of drivers. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 108, "Lamps, Reflective Devices, and Associated Equipment."
Patient related messages created in RayCare 3B, RayCare 4A will be lost when upgrading from RayCare 2 to RayCare 3B or later
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.
The firm received positive test results for Listeria monocytogenes during in house environmental sampling on one of their meat slicers.