State
72,971 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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
KICIMPRO kitchen faucets (model KM800-01-06BN) have been recalled because they leach lead into drinking water at levels that can harm infants and young children. About 50,000 units sold on Amazon from January 2024 through May 2025 are affected.
BASDEHEN kitchen faucets (model CFDTTH-000-YGH) sold on Amazon leak lead into drinking water at levels that can harm infants and young children's neurological development. About 24,000 units are affected.
VFAUOSIT kitchen faucets (model 06BNV) sold on Amazon leach lead and other contaminants into water at levels harmful to infants and young children. Consumers should stop using the faucets immediately.
General Motors is recalling certain 2023-2024 Cadillac LYRIQ vehicles because the driver video display may go blank while driving, hiding the speedometer, warning lights and rearview camera image.
Jayco is recalling certain 2020-2021 North Point fifth wheel travel trailers because the certification labels may have incorrect tire size information, leading owners to fit the wrong tires.
Tesla is recalling certain 2026 Model Y vehicles because the wiper arm hose connector may block the windshield washer nozzles, preventing washer fluid from reaching the windshield and reducing driver visibility.
Ethicon Endo-Surgery is recalling the Endopath Echelon Vascular White Reload surgical stapler due to reports of inadvertent instrument lockout during procedures. The lockout prevents cutting and stapling, potentially requiring conversion to open surgery; one patient death has been reported.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators nationwide because affected units may have open seals on the packaging, compromising sterility assurance.
Zydus Pharmaceuticals is recalling Esomeprazole Magnesium 40 mg delayed-release oral suspension because out-of-specification test results were found for unknown degradation products during stability testing.
PACCAR is recalling certain 2024-2026 Peterbilt 367, 548, 567 and 589 trucks because the rear brake piping assembly may have insufficient clearance, which can cause a loss of service brakes or ABS.
Hormel Foods is recalling approximately 256,185 pounds of Dinty Moore Beef Stew due to possible wood contamination. No injuries have been reported.
C.R. Bard is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Child) due to customer complaints that plastic plugs may be difficult or impossible to remove, preventing inflation of the gastric and esophageal balloons.
C.R. Bard Inc is recalling the Bard Single Intragastric Linton Balloon Tube (REF: 0092740) because users may be unable or find it difficult to remove plastic plugs needed to inflate the gastric and esophageal balloons.
C.R. Bard Inc is recalling the Bard Minnesota Four Lumen Esophagogastric Tamponade Tube (REF:0092220) because users may be unable to or have difficulty removing plastic plugs needed to inflate the gastric and esophageal balloons.
C.R. Bard Inc is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Intermediate, REF 0092300) due to reports that plastic plugs may be difficult or impossible to remove, preventing proper inflation of the gastric and/or esophageal balloons.
C.R. Bard is recalling Bard Blakemore Esophageal-Nasogastric Tubes (Adult) because users may find it difficult or impossible to remove the plastic plugs needed to inflate the gastric and esophageal balloons.
Philips is recalling MR 7700 model medical devices due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
AstraZeneca is recalling AIRSUPRA (albuterol sulfate and budesonide) inhalation aerosol due to a defective delivery system. The recall affects multiple lot numbers and expiration dates distributed nationwide.
Echopixel's TRUE 3D VIEWER SYSTEM may display imaging data with incorrect orientation (left/right/superior/inferior/anterior/posterior), which could lead to inaccurate measurements during clinical use.
Philips is recalling the SmartPath to dStream 3.0T medical device due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. This could affect image interpretation accuracy.
Philips is recalling certain Ingenia Ambition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application.
Cook Incorporated is recalling Check-Flo Performer Introducer devices because some units from affected lots may contain an incorrectly sized introducer sheath.
Echopixel's True 3D Viewer (Model EP-00003) with certain software versions can display ultrasound image orientation incorrectly, potentially leading to misdiagnosis or incorrect surgical planning.
Philips is recalling SmartPath to Ingenia Elition X MRI systems due to potential alignment errors in the cross reference line functionality when reviewing images generated with the MobiView application. The alignment errors could affect image interpretation.
Becton Dickinson is recalling certain BD Cathena Safety IV Catheter models due to a manufacturing defect that may create a hole in the septum, potentially causing blood leakage during insertion.