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.
Taro Pharmaceuticals is recalling 639,325 bottles of Ibuprofen Oral Suspension USP because they may contain small particles of inert plastic material introduced during manufacturing.
Taro Pharmaceuticals is recalling specific lots of Ibuprofen Oral Suspension USP because they may contain small particles of inert plastic material introduced during manufacturing.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension.
Mindray is recalling 14 Rosie4 Vital Signs Monitors because the NIBP valve assembly board contains software features not included in the current marketing clearance.
Mindray is recalling 107 Accutorr 7 Vital Signs Monitors because the NIBP valve assembly board contains software features not included in the current marketing clearance.
Anewmed Corporation is recalling 1,749 medical devices because the contract sterilizer lacked adequate packaging data to support the 2-year shelf life.
OrthoPediatrics Corp is recalling 969 Child Nail Attachment Bolts because they may bind with the intramedullary nail, potentially delaying surgical procedures.
OrthoPediatrics Corp is recalling 969 Adolescent Nail Attachment Bolts because binding between the bolt and nail may delay surgical procedures.
Mylan Pharmaceuticals is recalling 4,272 bottles of Prasugrel 5 mg tablets because they failed to meet dissolution specifications.
Keystone RV Company is recalling 2014 Springdale 253FWRLLS trailers because the Federal Identification Tag may list incorrect tire, rim, and axle sizes, potentially leading to unintentional overloading.
Sandoz Inc is recalling 76,644 bottles of Gatifloxacin Ophthalmic Solution 0.5% because the package insert is incorrect or missing.
Arbor Pharmaceuticals is recalling specific lots of Testosterone Cypionate Injection because shipper cartons were mislabeled, potentially causing confusion with different vial sizes.
Sandoz Inc is recalling Bimatoprost Ophthalmic Solution 0.03% because the package insert is incorrect or missing. The recall covers 346,929 bottles distributed nationwide.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Stryker Neurovascular is recalling Synchro2 guidewires because the product labels contain a typographical error in the millimeter dimension for the outer diameter.
Nephron Pharmaceuticals is recalling 19,390 syringes of Succinylcholine Chloride Injection because of incorrect or missing lot and expiration dates.
AuroMedics Pharma LLC is recalling one lot of Ranitidine Tablets USP, 150 mg, because some bottles were found to be empty.
Sandoz Inc. is recalling 346,929 bottles of Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension due to incorrect or missing package inserts.
Merritt Manufacturing is recalling Angel Guard Angel Ride car beds because the restraint harness may not be properly sewn, increasing injury risk in a crash.
McElrath Trailers is recalling 2014-2019 VX trailers because side marker LED lights may lack required reflex reflectors, reducing visibility.
KZRV is recalling 2019-2020 Connect and Sportsmen trailers because optional Rock Run rear storage racks may detach when loaded, creating a road hazard.
Arcimoto is recalling 2019 FUV vehicles because a wiring defect may cause a loss of traction power, increasing the risk of a crash.
Cooper Europe is recalling specific Avon Cobra Chrome motorcycle tires because a thin innerliner may cause rapid deflation, increasing crash risk.
Daimler Trucks is recalling 2,725 Western Star 4900 and 5700 trucks because sleeper cab vent windows may detach due to improper adhesive.