State
72,940 recalls have nationwide distribution and so reach Maryland. 8,218 additional recalls listed Maryland specifically in their distribution scope.
Of the 8,218 recalls naming Maryland we have scored against our rubric, 996 (12%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,131 (26%) are Severe.
Which agencies issued them
These figures cover only the 8,218 recalls whose distribution notice names Maryland specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lippert is recalling Q'Straint QRT-Max wheelchair restraints because the retractors may not lock, preventing proper securing of the wheelchair.
General Motors is recalling 1,120 GMC Canyon AT4X AEV vehicles because incorrect sensing and diagnostic module software may cause a second stage passenger air bag deployment when only a first stage is intended.
About 700 model year 2026 Trek Domane+ and Checkpoint+ electric bicycles are being recalled because the chainring bolts can come loose, causing the chainring to separate from the bike.
About 2,290 X-Pro Eagle and FRP Sahara 40cc youth ATVs are being recalled because their mechanical suspension fails safety requirements and the handlebars pose a laceration hazard.
About 2,650 Uuoeebb infant walkers are being recalled because they can fit through a standard doorway and fail to stop at the edge of a step, and their leg openings can entrap a child's head.
About 8,960 YCXXKJ baby bath seats are being recalled because they are unstable and can tip over while in use, posing a risk of serious injury or death due to drowning.
BMW of North America is recalling 36,922 model year 2025-2026 X3 vehicles because unexpected steering wheel rotation may occur while the vehicle is stationary.
American Nuts is recalling 2,700 units of Dry Roasted Baking Macadamia Nuts over potential Salmonella contamination. The FDA has classified the action as Class I.
Fresenius Kabi USA is recalling 483 cases of Ivenix LVP Primary Administration Sets after incorrect assembly of a specific lot that the firm states could result in serious patient injury.
Genepro Protein is recalling 250 bags of Genepro Whey 4th Generation protein because the labeling contains incorrect ingredient information and fails to declare milk as an allergen.
Lucid is recalling 2026 Gravity vehicles because incorrect seat covers may prevent side air bags from deploying correctly, increasing injury risk.
Bridgestone is recalling Firestone Destination LE3 tires because a belt edge insert may be out of position, causing tread separation and increasing crash risk.
Blue Bird is recalling 2026-2027 Vision and All American school buses because wheelchair restraints may fail to lock, increasing injury risk.
Philips North America is recalling the IntelliVue Patient Monitor MX700 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP90 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue MP40 over a potential issue where the monitors did not alarm.
Volkswagen is recalling 3,138 model year 2025 Tiguan vehicles because a fault in the passenger occupant detection system wiring may deactivate the front passenger air bag when the seat is occupied.
Philips North America is recalling the IntelliVue Patient Monitor MX450 over a potential issue where the monitors did not alarm.
Ventura Foods is recalling 3,556 cases of salad dressings sold under several brands after foreign objects, described as black plastic planting material, were found in granulated onion.
Philips North America is recalling the IntelliVue Patient Monitor MX550 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Multi-Measurement Module X3 over a potential issue where the monitors did not alarm.
Paragon 28 is recalling 20 Phantom Fibula Nails because out of specification thread depths may prevent the implant from mating with its mounting bolt, potentially requiring surgery to be aborted.
Philips North America is recalling the IntelliVue Patient Monitor MX100 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX600 over a potential issue where the monitors did not alarm.
Philips North America is recalling the IntelliVue Patient Monitor MX500 over a potential issue where the monitors did not alarm.