State
72,971 recalls have nationwide distribution and so reach North Dakota. 2,921 additional recalls listed North Dakota specifically in their distribution scope.
Of the 2,921 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 727 (25%) are Severe.
Which agencies issued them
These figures cover only the 2,921 recalls whose distribution notice names North Dakota specifically. The 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ascend Laboratories is recalling Cephalexin for Oral Suspension due to failed impurity specifications identified during stability testing. An out-of-specification result for Cephalexin Glucose Adduct was observed at six months.
AvKARE is recalling Chlorthalidone Tablets USP 25 mg due to failed dissolution specifications. The defect may affect the drug's therapeutic effectiveness.
R&M Refresher brand Instant Milk Tea Powder in Taro Flavor is recalled nationwide because the label does not declare milk, though the product contains Whey Powder and Sodium Caseinate derived from milk.
Ascend Laboratories is recalling Cephalexin for Oral Suspension due to an out-of-specification result in impurity testing that identified Cephalexin Glucose Adduct during stability analysis.
R&M Refresher Instant Milk Tea Matcha Flavor is recalled because its label declares "Non-Dairy Creamer" but does not specify that the product contains milk (whey powder and sodium caseinate). The product may cause allergic reactions in consumers with milk allergies.
Remel, Inc. is recalling one lot of Thermo SCIENTIFIC Sensititre Cation Adjusted AutoRead Mueller-Hinton Broth due to off-color that may affect performance of this in-vitro diagnostic device.
Turncare has recalled certain Guardian 2 System controllers because a software issue prevented "low" and "terminal" battery alerts from displaying on the screen in specific circumstances when the device was not running patient therapy.
Turncare is recalling Guardian System 2 Controllers due to a software issue where low and terminal battery alerts do not display on the screen in certain circumstances when the device is not running patient therapy.
Beckman Coulter is recalling certain DxI 9000 Access Immunoassay Analyzers due to incorrect motor/encoder and cable installation that causes error codes, prevents assays from running, and delays result generation.
BD BBL CultureSwab EZ Collection and Transport System (REF 220144) is being recalled because swabs may break during use. The recall affects units distributed nationwide in Maryland.
NOW Foods is recalling NOW Nutritional Yeast Powder (10 oz, UPC 7 33739 02460 2) because regular yeast was inadvertently packaged as nutritional yeast.
Glenmark Pharmaceuticals Inc., USA is recalling Ezetimibe and Simvastatin Tablets (10mg/40mg) due to out-of-specification results for related substances in a stability study. The recall affects approximately 6,759 bottles distributed nationwide.
Macleods Pharmaceuticals is recalling Levothyroxine Sodium 112 mcg tablets (Lot #MLF2401A, expiration 01/31/2026) distributed nationwide due to black hair found embedded in tablets.
FreshRealm is recalling chicken fettuccine alfredo products because Listeria monocytogenes contamination was found, resulting in 17 illnesses and 3 deaths.
Foretravel is recalling 2024-2026 Presidential Realm vehicles because engine vibration may cause rear kick up panel fins to detach, creating a road hazard.
Ford is recalling 2025 Bronco vehicles because a vent flap may prevent the passenger air bag from deploying, increasing injury risk in a crash.
Ford is recalling certain 2025 Super Duty trucks because the brake booster pushrod retaining spring may not have been installed, risking sudden loss of brake function.
Ford is recalling 2025 Mustang Mach E vehicles because the transmission park rod may fail to engage, creating a risk of vehicle rollaway and crash.
Ford is recalling certain 2022 Lincoln Navigator vehicles previously repaired under recall 22V455 because headlight control module software may fail the side marker and daytime running lights.
Ford is recalling 2021-2025 Mustang Mach E vehicles because electronic door latches may remain locked after exit, potentially trapping occupants.
Ford is recalling certain 2020-2025 Lincoln Aviator vehicles because rear door window bars and C-pillar trim may have insufficient adhesive bonding and detach.
Ford is recalling 2025 Ranger trucks because the instrument panel software may prevent critical safety warnings and gauges from displaying properly.
Ford is recalling certain 2020-2025 Explorer and Lincoln Aviator vehicles because the easy-entry second-row seat switch may bind, letting seats unlatch, fold or slide unexpectedly.
Ford is recalling 2025 Bronco four-door vehicles because the left-hand rear door may open from inside when the child safety lock is engaged, increasing injury risk.
Altec is recalling specific aerial and service trucks because a voltage spike may damage a control module, potentially causing a loss of vehicle control or brake performance.