State
72,992 recalls have nationwide distribution and so reach Virginia. 9,483 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,483 recalls naming Virginia we have scored against our rubric, 1,286 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,296 (24%) are Severe.
Which agencies issued them
These figures cover only the 9,483 recalls whose distribution notice names Virginia specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Evenflo is recalling Titan 65 child seats manufactured in early 2025 that may have incorrect instruction manuals, posing a risk of improper installation.
REV is recalling 2025-2026 Fleetwood Altitude and Holiday Rambler Incline motorhomes because water intrusion may cause electrical components to fail, potentially disabling carbon monoxide or propane detectors.
GoodSource Solutions is recalling Creamy Butter Sauce (Lot 701493) because the product was manufactured with recalled cilantro containing small wood-like pieces.
BD Texium Needle-Free Syringes (multiple sizes) may leak at the interface between the male luer component and needle-free connector, potentially causing treatment delays, medication underdosing, or exposure to hazardous drugs.
Sysco Corporation is recalling cucumber products sold under the Imperial Fresh, East Coast Fresh, Just Cut, Wellsley Farms, and other brands due to potential Salmonella contamination. The products were distributed to multiple states and Puerto Rico.
The EPIONE Model 30-0001 stereotactic device is recalled due to a software bug that may cause the robotic arm to incorrectly guide surgical instruments during CT-guided ablation procedures. Four units have been distributed in the U.S.
Natus Neurology has recalled the OBM00002 OBM DAB (Digital Acquisition Box) because electrode placement labels were applied backwards. This may lead to misdiagnosis of seizure location in neonates monitored with the device.
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.
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.
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.
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.
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.
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.
AvKARE is recalling Chlorthalidone Tablets USP 25 mg due to failed dissolution specifications. The defect may affect the drug's therapeutic effectiveness.
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.
Baxter is recalling certain Novum IQ Syringe Pumps manufactured or repaired after July 4, 2023, due to a design issue that may falsely detect a syringe flange when none is loaded, causing the pump interface to become stuck or display a System Error 21502.
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.
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.
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 2025 Mustang Mach E vehicles because the transmission park rod may fail to engage, creating a risk of vehicle rollaway and crash.