State
72,936 recalls have nationwide distribution and so reach Virginia. 9,479 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,479 recalls naming Virginia we have scored against our rubric, 1,285 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,294 (24%) are Severe.
Which agencies issued them
These figures cover only the 9,479 recalls whose distribution notice names Virginia specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Altruan GmbH is recalling the Clearest Strep-A Cassette Test, used to detect group A streptococci in throat swab samples, because the product is not cleared by the FDA.
Medline is recalling three surgical kits containing Cardinal Health Aqua-Seal Chest Drainage Units because the instructions for use have been updated to clarify the target patient population as adults.
Penner Patient Care is recalling Pacific Bathing Spa models 760010-1 and 770010-1 because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa model 360020-1EP because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa models in the 350010 series because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa model 360020-1P because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa models in the 361910 series because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa models in the 360030 series because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa models 390010-1, 390010-X and 390010-2 because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa models in the 560010 series because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa model 860010-1L because the device does not bear a unique device identifier.
Penner Patient Care is recalling Pacific Bathing Spa models across the 360010, 362010 and 370000 series because the device does not bear a unique device identifier.
Ford is recalling certain 2020-2022 F-Super Duty and related vehicles previously repaired under recall 24V957 because biodiesel deposits may form on pump drivetrain rollers, leading to fuel pump failure.
Hyundai is recalling 2026 Palisade and Palisade Hybrid vehicles with Limited or Calligraphy trim because the second and third row power seats may fail to detect a person and continue moving, risking entrapment or injury.
Ford is recalling certain 2020-2026 Explorer and Lincoln Aviator vehicles because the seat belt anchor bolts at the second-row outer seating positions may be improperly secured.
Ford is recalling certain 2025–2026 Maverick vehicles because the moonroof glass may not be bonded correctly to the frame and could detach, becoming a road hazard and increasing crash risk.
Forest River is recalling 2025-2026 Entourage motorhomes because the cargo capacity label may incorrectly state 7 seat-belted positions instead of 8, risking vehicle overload.
Ford is recalling certain 2025-2026 F-59 and F-53 commercial stripped chassis vehicles because the exterior brake lights may remain illuminated when the driver is not applying the brakes.
Tiffin is recalling 2025-2026 GT1, GH1, and 2026 GH2 motorhomes because incorrect seat belt labels may lead to unbelted passengers.
Ferrari is recalling 2025-2026 12Cilindri vehicles because rear and side windows have insufficient light transmittance, which can impair driver visibility and increase crash risk.
Orange EV is recalling 2022-2026 terminal trucks because the optional foldaway training seat may fail, potentially failing to restrain occupants during a crash.
New Flyer is recalling certain 2021-2026 transit buses because an inverter software error may cause unintended acceleration or deceleration.
Micro Bird is recalling 2002-2026 transit buses because an installation error may prevent wheelchair tie-downs from locking, increasing injury risk.
Micro Bird USA LLC is recalling 2026 G5 transit buses because an installation error may prevent wheelchair tie-downs from locking, increasing injury risk.
Micro Bird is recalling certain school buses because an installation error may prevent wheelchair tie-downs from locking, increasing injury risk.