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.
Honda is recalling Genuine Accessory Rear Carriers for 2019-2020 Monkey motorcycles because they may fail under load, posing a crash risk.
Dorel is recalling 28,800 Babidéal Storm Booster Car Seats sold at Family Dollar because the fabric cover may lack required safety warnings, increasing crash injury risk.
Subaru is recalling 2017 Impreza vehicles because a defective PCV valve may break apart and enter the engine, causing a loss of power while driving.
Subaru is recalling 2017-2018 Impreza and 2018 Crosstrek vehicles because the PCV valve may break apart, potentially causing a loss of power while driving.
GCP Laboratories is recalling Major Infants' Gas Relief Drops due to microbial contamination of the non-sterile product.
Becton, Dickinson and Company is recalling 22 BD FACSLyric Flow Cytometers because they may produce falsely high absolute counts when used with BD Trucount Tubes.
Sandoz is recalling 13,130 bottles of Ranitidine Hydrochloride Capsules 150mg because a trace amount of the impurity NDMA was detected.
Sandoz is recalling specific lots of Ranitidine Hydrochloride Capsules 150mg because a trace amount of the impurity NDMA was detected.
Morton Grove Pharmaceuticals is recalling Prednisolone Sodium Phosphate Oral Solution because it failed impurity specifications for Prednisolone Impurity 14.
Porsche is recalling 2017-2020 Cayenne and Panamera vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out.
Unipharma is recalling DrKids Himasal Natural Nasal Saline Solution vials due to a precautionary measure regarding potential contamination with B. cepacia bacteria.
BMW is recalling 2020 X3 M40i and X4 M40i vehicles because the steering rack pinion teeth may break, causing a loss of steering control.
Becton Dickinson is recalling 115,200 CareFusion MaxPlus Clear Needleless Connectors because the valve may fail to close, posing risks of blood loss and air embolism.
Airstream is recalling 2019-2020 Atlas motorhomes because incorrect wiring may cause overheating and fire. Dealers will correct the wiring free of charge.
Sandoz is recalling Ranitidine Hydrochloride Capsules 300mg because a trace amount of the impurity NDMA was detected.
Forest River is recalling 2020 Sunseeker, Freelander, and Leprechaun vehicles because the seatbelt warning light may not illuminate, increasing crash injury risk.
Centurion Medical is recalling CVC Bundle VanTex kits because the included BD MaxZeroNeedleess Connector may release fluid droplets after disconnection.
Pfizer is recalling 17,832 bags of LMD in Dextrose Injection due to a potential leak that compromises sterility.
Roche Diagnostics is recalling Tina-quant sTfR assays due to updated claims regarding rheumatoid factor interference.
AZIYO BIOLOGICS is recalling CanGaroo Envelopes because sutures may become brittle or break before expiration. The devices are used to secure cardiac and neurostimulator implants.
Becton Dickinson is recalling BD Microtainer SST tubes because damaged reservoirs may cause insufficient sample volume and erroneous test results.
Diamond Crystal Brands is recalling Chef's Companion Instant Chocolate Mousse Mix because it contains soy lecithin that is not declared on the label.
Centurion Medical Products is recalling Triple Lumen CVC kits because the included BD MaxZeroNeedleess Connector may allow fluid droplets to separate from the sealed surface after disconnection.
Centurion Medical Products is recalling OR VANTEX kits because the included BD MaxZeroNeedleess Connector may allow fluid droplets to separate after disconnection.
Epic Pharma is recalling Estradiol 0.5 mg tablets because 1 mg tablets were found in the bottles. Patients should stop using the product and contact their healthcare provider.