State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Red Mountain Compounding Pharmacy is recalling specific lots of S-DMSO 6.25% ophthalmic solution because the product lacks assurance of sterility.
GE Healthcare is recalling 59 Giraffe OmniBed Carestation CS1 devices because fasteners may be under-torqued, posing a risk that the canopy could detach and fall.
Red Mountain Compounding Pharmacy is recalling specific lots of lidocaine and phenylephrine injection syringes due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Dextrose 50% vials because the FDA cannot ensure the product is sterile.
Red Mountain Compounding Pharmacy is recalling S-Dexpantenol injection vials due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-TRIMIX injection vials because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of S-Estradiol Cypionate injections due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-TRIMIX injection vials because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling specific lots of S-TEST CYP/PROP 160/40MG/ML MDV in sesame oil due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling 81 vials of S-HCG 1200U/ML injection solution because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Vit A Palmitate 50,000 IU/mL corn oil due to a lack of assurance of sterility.
ICU Medical is recalling 389,808 bags of Lactated Ringer's Injection due to the presence of particulate matter. The affected product was distributed nationwide.
Images Unlimited Products is recalling Cellect and Essentials Factor multi-mineral supplements due to unsafe levels of arsenic and lead.
ICU Medical Inc is recalling 0.9% Sodium Chloride Injection USP bags because of the presence of particulate matter in the solution.
Red Mountain Compounding Pharmacy is recalling specific lots of S-TEST CYP/PROP 160/40MG/ML MDV in Ethyl Oleate due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Testosterone Ultra 250mg/ml vials because the product lacks assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-MIC 25/50/50MG/ML MDV SOLN vials nationwide due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-Ascorbic/Glutathione 1.25/1.25% Ophthalmic Solution due to a lack of assurance of sterility.
Red Mountain Compounding Pharmacy is recalling S-TEST CYP 200mg/ml vials nationwide due to a lack of assurance of sterility.
Zimmer Biomet is recalling 5.4 million custom medical devices because non-highly polished implants may adhere to the LDPE bag packaging.
Argon Medical Devices is recalling specific lots of sterile double female and male luer lock adapters because incomplete pouch seals may compromise sterility.
Insulet Corporation is recalling 264 units of the Omnipod DASH Insulin Management System because a communication interruption may cause inaccurate insulin data to be displayed.
Western / Scott Fetzer is recalling 486 Grab n Go Opti VIPR oxygen systems because the control knob may rotate beyond its functional range, limiting access to flow settings.
Red Mountain Compounding Pharmacy is recalling S-Procaine HCL 2% Buffered due to a lack of assurance of sterility. The affected prescription products were distributed nationwide.
Daimler Trucks is recalling 2019 Freightliner Business Class M2 electric vehicles because a software error may cause unexpected movement, increasing crash risk.