State
73,809 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.
Of the 4,483 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (23%) are Severe.
Which agencies issued them
These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mako Surgical Corporation is recalling specific lots of the Stryker Mako Vizadisc Knee Procedure Tracking Kit because the reflective material may be damaged, preventing camera detection.
Stryker is recalling AXS PP Burr Hole Covers because the sterile packaging may become compromised after three years, potentially affecting sterility.
Stryker is recalling QUIKFLAP cranium plates because the sterile packaging may become compromised after three years.
Pfizer is recalling 17,136 bottles of Children's Advil Suspension because the included dosage cup is marked in teaspoons while the label instructions use milliliters.
Stryker is recalling 22,831 AXS PP cranium plates because the sterile packaging may become compromised after three years.
Stryker is recalling QUIKFLAP burr hole covers because the sterile packaging may become compromised after three years.
Stryker is recalling QuickFlap Sterile Procedure Packs because the sterile barrier may become compromised after three years.
Validus Pharmaceuticals is recalling 7,864 bottles of Calcitriol Oral Solution because testing showed lower than expected potency at the 18-month stability time point.
Stryker is recalling QUIKFLAP burr hole covers because the sterile packaging may become compromised after three years, potentially affecting sterility.
Stryker is recalling AXS PP burr hole covers because the sterile packaging may become compromised after three years, potentially affecting sterility.
Stryker is recalling QuickFlap Sterile Procedure Packs because the sterile barrier may become compromised after three years.
Stryker is recalling 22,831 AXS PP cranium plates because the sterile packaging may become compromised after three years.
Morton Salt Inc. is recalling 22,284 units of Morton Natural Sea Salt because iodized sea salt was packaged in the wrong containers.
Akorn, Inc. is recalling specific lots of Azelastine HCl Ophthalmic Solution 0.05% because of out-of-specification results for Azelastine N-oxide.
Validus Pharmaceuticals is recalling 696 bottles of Rocaltrol (calcitriol) Oral Solution because testing showed lower than expected potency.
Mayne Pharma is recalling 6,456 bottles of Oxycodone and Acetaminophen Tablets due to a lot number labeling error on the primary container.
Collins Bus is recalling 2012-2018 school buses with Ricon wheelchair lifts because a cam may fail, causing the platform to rise too high and increasing injury risk.
Midwest Fire is recalling 2017-2019 emergency vehicles because Whelen brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Bridgestone is recalling specific commercial tires because exposed sidewall steel cords can cause rapid air loss, increasing crash risk.
Ford is recalling 2015-2018 F-150 Regular Cab and SuperCrew Cab vehicles because seat belt pretensioner sparks may ignite B-pillar materials, posing a fire risk.
Daimler Trucks is recalling 2016-2019 FCCC chassis because a damaged module may cause rear lights to fail, increasing crash risk.
Eldorado is recalling 2012-2018 transit buses because a wheelchair lift cam may fail, allowing the platform to rise too high and increase injury risk.
General Motors is recalling 2015-2016 Chevrolet and GMC vehicles because a brake pedal pivot nut may loosen, potentially rendering the brakes inoperative or interfering with the accelerator.
Daimler Trucks is recalling 2017-2019 Freightliner and Western Star trucks because a restricted fuel pump cooling circuit screen may cause the fuel line to burst, leading to fuel leaks or engine stalling.
General Motors is recalling 2018-2019 Chevrolet, GMC, Buick, and Cadillac vehicles because rear brake caliper pistons may have insufficient coating, potentially reducing braking performance.