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All product recalls associated with MERCEDES-BENZ.
Total Recalls
1000
Past Year
433
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.
Daimler Vans USA, LLC (DVUSA) is recalling certain 2016-2021 Mercedes-Benz Metris vehicles. The brake fluid reservoir may be incorrectly mounted, which can allow it to detach.
Marketed Without An Approved NDA/ANDA: Product was found to contain undeclared sildenafil and tadalafil, ingredients found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.
May show unexpected locus specific signals in addition to those at 14q32.
Illegal importation of COVID-19 AG Test kits into the U.S. The COVID-19 Ag Test are not approved, cleared or authorized for distribution within the U.S.
Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2021 AMG GT Black Series vehicles. The wiring harness for the front wheel speed sensor may be the incorrect length, which could result in damage to the harness during certain driving conditions.
Distribution of Defibrillators that are not approved or cleared for distribution US Market.
Undeclared eggs
Undeclared eggs
There is a potential to leak from the catheter where it connects to the drain bag
This recall involves bottles of Geri-Care Brand over-the-counter acetaminophen and aspirin. The acetaminophen is 500mg with 1,000 tablets in the bottle. The aspirin was sold in 81mg with 300 and 1,000 tablets in the bottle and 325mg with 250 and 1,000 tablets in the bottle. Product Count Extra Strength Acetaminophen 500mg Tablets 1,000 Regular Strength Enteric Coated Aspirin 325mg Tablets 250 Regular Strength Enteric Coated Aspirin 325mg Tablets 1,000 Adult Low Dose Enteric Coated Aspirin 81mg Tablets 300 Adult Low Dose Enteric Coated Aspirin 81mg Tablets 1,000
Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
In instances where custom reference ranges were configured on the device post installation, a possibility to inadvertently apply changes to reference range values was found on software versions 2.59.3 and all earlier versions, which can potentially lead to displaying and printing incorrectly-configured reference range values
Laparoscopic devices have a sterile symbol included on labels but devices are non-sterile.
The FRIGG silicone pacifiers came in two designs: Classic and Daisy. The Classic design consists of a silicone nipple attached to a round plastic shield. The Daisy design consists of a silicone nipple attached to a round scalloped plastic shield. Each design came in two sizes: 0-6 months and 6-18 months. The name "FRIGG" appears in raised letters on the handle of the pacifier shield. The FRIGG silicone pacifiers were sold in over 40 colors.
Incorrect marketing label (25 mm) was applied to product size 20 mm.
individual components have been labelled with incorrect colours. The red and green colours are opposite to those specified in the product labelling. The EGR1 probe is labelled in green rather than red and the control probe labelled in red rather than green. The expected positive signal pattern in the case of 1x deleted 5q will be 1G2R instead of 1R2G, an incorrect result
Failed Dissolution Specifications.
This recall involves Bella residential elevators manufactured from 2009 to 2021. Models include Symmetry IGD, Hydraulic, and Winding Drum Elevators. The Symmetry brand name is located on the elevators' controllers. The elevators are used in consumers' homes.
This recall involves Inclinator residential elevators manufactured from 1979 through 2021. Models include: Winding Drum (450 - 1,000 lb.), Hydraulic Drive, Chain Drive, Traction Drive and Overhead Cable Drum. Serial numbers are located on the elevator controllers, stamped on the rails, or on the outside of the drum for Winding Drum units. The elevators are used in consumers' homes.
Wheel spoke may crack causing the wheel to separate from the axle may result in patient injuries, including bruising and lacerations requiring stitches.