State
73,741 recalls have nationwide distribution and so reach New Hampshire. 4,482 additional recalls listed New Hampshire specifically in their distribution scope.
Of the 4,482 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 1,048 (23%) are Severe.
Which agencies issued them
These figures cover only the 4,482 recalls whose distribution notice names New Hampshire specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Better Made Snack Foods is recalling 660 bags of Original Potato Chips due to undeclared milk. The product was sold in Michigan, Ohio, and via mail order nationwide.
Chrysler is recalling 2019 Jeep Renegade and Fiat 500X vehicles because incorrect software may disable passive safety features, increasing injury risk in a crash.
Spartan Motors is recalling 2012-2018 Utilimaster Reach vehicles because improper electrical grounding may cause windshield wipers to stop working, reducing visibility.
KTM and Husqvarna are recalling about 780 model year 2019 50 SX and TC 50 motorcycles because the throttle can stick open, posing a crash hazard.
Zimmer Biomet is recalling 809 units of RingLoc Hip System Self-Tapping Bone Screws due to a potential packaging error where 30mm screws may be labeled as 20mm and vice versa.
Century Snacks LLC is recalling Snak Club Honey Bliss Nut Mix because the Honey Butter Seasoning contains milk, a major allergen, that was not declared on the packaging.
Zimmer Biomet is recalling 809 units of RingLoc Hip System Self-Tapping Bone Screws because 30mm screws may have been packaged as 20mm screws, and vice versa.
Zimmer Biomet is recalling 89 units of the Small Diameter Cement Plug Inserter due to a lack of adequate sterilization validation.
North Central Emergency is recalling 2016-2018 ambulances because brake lights may illuminate without the pedal being pressed, potentially confusing other drivers.
Fungi Perfecti LLC is recalling Host Defense MycoBotanicals Blood Sugar dietary supplements because they contain undeclared wheat. The recall affects 11,042 bottles distributed in the US, Canada, and Norway.
Toyota is recalling 2019 Lexus ES vehicles because the driver knee air bag assembly may have been improperly installed, potentially affecting deployment in a crash.
Johnson Matthey Inc. is recalling Morphine Sulfate USP Milled API due to bioburden out of specification results.
KRS Global Biotechnology is recalling 190 bags of Repinephrine 16 mg IV solution due to a label mix-up. The product was distributed nationwide.
Abbott Laboratories is recalling specific lots of ARCHITECT Creatine Kinase IVD kits due to a stability issue that may cause error codes or out-of-range quality control results.
Jubilant Cadista Pharmaceuticals is recalling 12,960 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on the tablet edges.
Conformis, Inc. is recalling two iTotal Posterior Stabilized Knee Replacement Systems because the box and sterile pouch labels did not match the contents.
Pfizer is recalling specific lots of Clindamycin Injection due to high out-of-specification impurity results at the 24-month time point.
Pfizer is recalling specific lots of Cleocin Phosphate injection because high levels of impurities were found at the 24-month time point.
Pfizer is recalling specific lots of Clindamycin Injection because high out-of-specification impurities were found at the 24-month time point.
Pfizer is recalling specific lots of Clindamycin Injection because high levels of impurities were found at the 24-month time point.
KRS Global Biotechnology is recalling 433 bags of NORepinephrine 4 mg in 5% Dextrose due to a label mix-up. The product was distributed nationwide.
Abbott Laboratories is recalling 30 kits of ARCHITECT Creatine Kinase IVD due to a stability issue that may cause error codes or out-of-range quality control results.
Abbott Laboratories is recalling 6,353 CELL-DYN Emerald analyzers worldwide because they may generate incorrect low quality control results for red blood cells and platelets.
Pfizer is recalling specific lots of Cleocin Phosphate injection because high out-of-specification impurity levels were detected at the 24-month time point.
Beaver Visitec is recalling 97 boxes of Micro Knife 5.0mm 30° instruments because the expiration date was misprinted as the lot number.