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.
Cardinal Health 200, LLC is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.
Cardinal Health is recalling Monoject Standard Hypodermic Needles due to a manufacturing defect that could compromise the sterility barrier.
Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Cardinal Health 200, LLC is recalling Monoject Blunt Cannula 22 G x 1-1/2" (Item code: 8881202389) because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Siemens is recalling 89 Artis zee multi units because a power supply issue may cause the X-ray generator to fail during procedures.
Cardinal Health 200, LLC is recalling Monoject Blunt Cannulas because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Cardinal Health is recalling Monoject Standard Hypodermic Needles because a manufacturing defect in the cartridge component could compromise the product's sterility barrier.
Geritrex, LLC is recalling Gericare Iron Supplement Elixir due to cGMP deviations that may have resulted in microbial contamination.
Deva Holding AS is recalling Temozolomide Capsules due to manufacturing deviations that allowed possible cross-contamination with beta-lactam products.
Cardinal Health is recalling Monoject 201 Vet Pak Hypodermic Needles due to a manufacturing defect that could compromise the product's sterility barrier.
Siemens is recalling 32 AXIOM Artis dMP units because a power supply tolerance issue may cause the X-ray generator to fail during procedures.
Siemens Medical Solutions is recalling 428 Artis zee ceiling units due to a power supply tolerance issue that may cause generator failure and prevent X-ray production.
Siemens is recalling 178 AXIOM Artis dTA units due to a power supply issue that may prevent X-ray generation during procedures.
Siemens Medical Solutions is recalling 170 Artis zee floor units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Siemens is recalling 268 Artis zee biplanes because a power supply tolerance issue may cause generator failure, preventing X-ray production during procedures.
Abbott Laboratories is recalling 11,063 Immunoglobulin G in vitro diagnostic kits to update instructions for use regarding reagents and specimen handling.
Getinge US Sales LLC is recalling seven PulsioFlex Monitoring Systems because they display an internal error message requiring restart or service.
Medical Intelligence Medizintechnik GmbH is recalling iGuide System software versions 2.2.0, 2.2.1, and 2.2.2 because the Constant Correlation Check may incorrectly demand verification scans.
Siemens is recalling 24 AXIOM Artis MP units because a power supply tolerance issue may cause generator failure, preventing X-ray procedures.
Abbott Laboratories is recalling 8,037 C4 in vitro diagnostic assay kits to update the Instructions for Use (IFU) regarding reagents and specimen handling.
Terumo Medical Corporation is recalling 638,000 Sur-vet Needles due to a potential loss of package integrity that may compromise sterility.
Becton Dickinson is recalling 3mL Luer-Lok syringes because the scale markings were printed incorrectly, resulting in missing or partially printed numbers and lines.
Pharma-Natural Inc. is recalling Lid O Creme topical analgesic cream because it was manufactured with current good manufacturing practice violations, including lack of process validation.
Siemens is recalling five AXIOM Artis FC units due to a power supply tolerance issue that may cause generator failure and prevent X-ray imaging.
Deva Holding AS is recalling Temozolomide capsules due to manufacturing deviations that allowed possible cross-contamination with beta-lactam products.