State
73,596 recalls have nationwide distribution and so reach Virginia. 9,495 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,495 recalls naming Virginia we have scored against our rubric, 1,284 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,697 (28%) are Severe.
Which agencies issued them
These figures cover only the 9,495 recalls whose distribution notice names Virginia specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Grech is recalling 2026-2027 Strada, Terreno, and Turismo motorhomes because a rooftop ventilation fan circuit board may overheat and cause a fire.
Highland Ridge RV is recalling 2022-2024 Range Lite Air travel trailers because fastener failure may cause the fresh water tank to detach, creating a road hazard.
Sterling Pharmaceutical Services is recalling Sodium Chloride Hypertonicity Ophthalmic Solution, 5%, due to a lack of assurance of sterility.
Sterling Pharmaceutical Services LLC is recalling specific lots of Lubricating Tears because the company cannot guarantee the product is sterile.
Sterling Pharmaceutical Services LLC is recalling Gentle Eyes Lubricant Eye Drops due to a lack of assurance of sterility.
Sterling Pharmaceutical Services LLC is recalling Major LubriFresh P.M. Nighttime Ointment due to a lack of assurance of sterility. The recall covers 34,368 tubes distributed nationwide.
Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution due to a lack of assurance of sterility.
Medline Industries is recalling 128 Major Pack Convenience Kits containing neurological sponges due to potential endotoxin variability that may cause adverse health events.
Olympus is recalling 404 BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Sterling Pharmaceutical Services LLC is recalling AvKare Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% due to a lack of assurance of sterility.
Insight Pharmaceuticals is recalling 2.3 million bottles of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.
Insight Pharmaceuticals is recalling specific lots of Clear Eyes Redness Relief eye drops due to a lack of assurance of sterility.
Sterling Pharmaceutical Services LLC is recalling Walgreens Lubricant Eye Drops due to a lack of assurance of sterility. Consumers should stop using the product.
Volkswagen is recalling 2023-2026 ID.4 vehicles because the high voltage battery may fail and cause a vehicle fire, increasing the risk of injury.
Boston Scientific is recalling Imager II Angiographic Catheters because the tip may fracture or detach, potentially causing device fragments to remain in or migrate through the patient's vasculature.
CooperSurgical is recalling 149 boxes of INCA Neonatal Nasal CPAP replacement sets because the flexible tubing may disconnect from the nasal cannula, potentially reducing treatment effectiveness.
Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.
Olympus is recalling 105 BiCOAG Hemostasis Probes because a manufacturing defect may cause the ceramic tip to detach during use.
Olympus Corporation of the Americas is recalling 816 units of BiCOAG Hemostasis Probes because the ceramic tip may detach due to insufficient adhesive.
Philips is recalling 219 EPIQ Elite Diagnostic Ultrasound Systems due to a software issue that may cause inaccurate blood flow velocity measurements and potential misdiagnosis.
Becton, Dickinson and Company is recalling 15,455 ForeSight Elite Tissue Oximetry Cables due to incorrect switching of Channel 1 and 2 on the module and flag labels.
Heidelberg Engineering is recalling 87 SPECTRALIS units with Flex Modules because wheels may detach, causing the stand to tip over and injure nearby people.
Maquet is recalling 667 PowerLED 300 Concealed Lighting Systems because the spring arm may detach and fall, posing a potential injury risk.
Abiomed is recalling 3,322 Automated Impella Controllers worldwide due to firmware and software defects that affect pressure signal accuracy and system reliability.
Medline is recalling Healthmark Instrument Channel Brush kits due to potential sharp edges that could cause cuts, abrasions, or infection.