State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Aurobindo Pharma USA Inc. is recalling specific lots of Simvastatin 40mg tablets because they were manufactured in an area with observed water leakage.
Canon Medical System is recalling 10 Aquilion Prime CT scanners because a software error may interrupt scanning and prevent normal shutdown, resulting in data loss.
Shanghai United Imaging Healthcare is recalling two uMI 550 PET/CT systems due to software bugs that may cause reconstruction problems and patient rescans.
B&B Pharmaceuticals is recalling Estradiol USP powder because Teflon was found in the product. The recall covers 3,825 grams distributed nationwide.
Canon Medical System is recalling two Aquilion Premium CT scanners because a software error can interrupt scans and cause loss of raw data.
Boddingtons Plastics Ltd is recalling Endocuff Vision models ARV 110, 120, 130, and 140 to update instructions regarding contraindications and potential complications.
Canon Medical System is recalling two Aquilion One CT scanners because scanning errors may interrupt exams and force system reboots, resulting in the loss of acquired raw data.
Merit Medical Systems is recalling six units of nonsterile ChloraPrep applicators that were inadvertently shipped to a customer in Illinois.
Filltech USA is recalling Dermatone Sunscreen Lotion due to positive tests for yeast and bacteria.
Filltech USA is recalling Dermatone Sunscreen Lotion SPF 50 due to positive tests for yeast and bacteria.
Boston Scientific is voluntarily recalling 118 units of Nitinol Thermocouple Electrodes because they were packaged with incorrect Instructions for Use.
Canon Medical System is recalling one Aquilion Precision CT scanner because a software error may interrupt scanning and cause loss of raw data.
Aurobindo Pharma USA Inc. is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because they were manufactured in an area with observed water leakage.
Canon Medical System is recalling one Aquilion One Vision CT scanner because a software error can interrupt scans and cause loss of raw data.
Boston Scientific is voluntarily correcting 40 units of Nitinol Thermocouple Electrodes because they were packaged with an incorrect revision of the Instructions for Use.
Aurobindo Pharma USA Inc. is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because they were manufactured in an area with observed water leakage.
Life Technologies is recalling 35 units of the Oncomine Dx Target Test because the expiration date was extended prior to clearance.
Aurobindo Pharma USA Inc. is recalling Mirtazapine Tablets 15mg due to water leakage observed in the manufacturing area.
Life Technologies is recalling 79 units of the Ion Torrent Dx No Template Control Kit due to extended expiration dates prior to clearance.
Aurobindo Pharma USA Inc. is recalling specific lots of Acetaminophen and Codeine Phosphate tablets because they were manufactured in an area with observed water leakage.
Life Technologies is recalling 66 units of the Oncomine Dx Target Test RNA Control because the expiration date was extended prior to regulatory clearance.
Aurobindo Pharma USA Inc. is recalling specific lots of Oxycodone and Acetaminophen tablets because they were manufactured in an area with observed water leakage.
Canon Medical System is recalling six Aquilion Lightning CT scanners because a software error can interrupt scanning and prevent normal shutdown, causing loss of raw data.
Boston Scientific is voluntarily recalling 110 Nitinol Thermocouple Electrodes because they were packaged with incorrect Instructions for Use.
Boston Scientific is voluntarily correcting 437 units of Nitinol Thermocouple Electrodes because they were packaged with an incorrect revision of the Instructions for Use.