State
73,738 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,849 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,245 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Conversio Health is recalling Formoterol 12mcg / Budesonide 0.5mg inhalation vials nationwide due to a lack of processing controls.
Washington Homeopathic Products, Inc. is recalling Natrum Phosphoricum 6X Tablets because they were not manufactured under current good manufacturing practices.
Washington Homeopathic Products, Inc. is recalling StellaLife VEGA Oral Gel Rinse because it was not manufactured under current good manufacturing practices.
Washington Homeopathic Products is recalling Magnesia Phosphorica 6X tablets because they were not manufactured under current good manufacturing practices.
Cincinnati Sub-Zero is recalling 3,932 Blanketrol III Hyper-Hypothermia Systems to add warnings about tissue damage from extended high temperatures and clarify automatic mode usage.
Washington Homeopathic Products, Inc. is recalling Calcarea Sulphurica 6X Tablets because they were not manufactured under current good manufacturing practices.
Washington Homeopathic Products, Inc. is recalling Natrum Sulphuricum 6X tablets because they were not manufactured under current good manufacturing practices.
Cook Inc. is recalling 135 Torcon NB Advantage Catheters because undersealed packaging pouches may compromise sterility. The devices are distributed worldwide.
Washington Homeopathic Products is recalling Pareira (Brava) 1X Tincture because it was not manufactured under current good manufacturing practices.
Conversio Health is recalling Albuterol, Ipratropium, and Budesonide inhalation vials nationwide due to a lack of processing controls.
Washington Homeopathic Products, Inc. is recalling 489 bottles of Calcarea Fluorica 6X Tablets because they were not manufactured under current good manufacturing practices.
Cook Inc. is recalling 41 units of Pneumothorax Trays because a perforation line may be positioned over the sterile area, potentially compromising device sterility.
Conversio Health is recalling Albuterol 2.5mg / Ipratropium 0.75mg vials nationwide due to a lack of processing controls.
Washington Homeopathic Products, Inc. is recalling Ferrum Phosphoricum 6X Tablets because they were not manufactured under current good manufacturing practices.
Conversio Health is recalling Albuterol, Ipratropium, and Triamcinolone inhalation vials due to a lack of processing controls.
Washington Homeopathic Products, Inc. is recalling Natrum Muriaticum 6X Tablets because they were not manufactured under current good manufacturing practices.
Conversio Health is recalling Albuterol and Ipratropium inhalation vials nationwide due to a lack of processing controls.
Washington Homeopathic Products, Inc. is recalling 295 bottles of Kali Sulphuricum 6X Tablets because they were not manufactured under current good manufacturing practices.
Washington Homeopathic Products, Inc. is recalling R2103 homeopathic product because it was not manufactured under current good manufacturing practices.
Washington Homeopathic Products, Inc. is recalling 417 bottles of Kali Phosphoricum 6X Tablets because they were not manufactured under current good manufacturing practices.
Conversio Health is recalling Albuterol, Ipratropium, and Budesonide inhalation vials due to a lack of processing controls.
Neocis Inc. is recalling three units of the Neocis Guidance System Fiducial Array because they may mismatch measurement files, resulting in a failed landmark check.
Angiodynamics Inc. is recalling BIOFLO 8F Single Titanium Non-Filled Valved ports because snap lock connectors may not meet specifications, preventing catheter insertion and delaying implantation.
Washington Homeopathic Products, Inc. is recalling Kali Muriaticum 6X Tablets because they were not manufactured under current good manufacturing practices.
X-Gen Pharmaceuticals is recalling Levetiracetam Injection vials because the incorrect package insert version was attached to the product.