State
73,809 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.
Of the 7,851 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 2,246 (29%) are Severe.
Which agencies issued them
These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling ALTRUA 2 SR pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Users should check for discoloration or yellowing of the protective seal.
Boston Scientific is recalling VISIONIST X4 CRT-P Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Unichem Pharmaceuticals is recalling Divalproex Sodium tablets because metronidazole powder was found in one bottle. The product was distributed nationwide.
Boston Scientific is recalling ALTRUA 2 EL DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Ventura Foods is recalling specific lots of honey mustard dressing because a plastic foreign object was inadvertently introduced into the product stream.
Ventura Foods is recalling specific lots of Imperial, Classic Gourmet, and Culinary Secrets tartar sauces because a plastic foreign object was introduced into the product stream.
Ventura Foods, LLC is recalling Rio Pacific Foods Deluxe BBQ Sauce because a plastic foreign object was inadvertently introduced into the product stream.
Shiseido America Inc. is recalling bareMinerals Broad Spectrum SPF 50 Daily Prep Lotion because the manufacturing of active pharmaceutical ingredients did not meet GMP and quality requirements.
Ventura Foods is recalling 117 cases of House Recipe Ranch Dressing & Dip because a plastic foreign object was inadvertently introduced into the product stream.
Ventura Foods, LLC is recalling various French dressings because a plastic foreign object was inadvertently introduced into the product stream.
Ventura Foods is recalling specific lots of Gordon Choice Thousand Island Dressing because a plastic foreign object was inadvertently introduced into the product stream.
Valeant Pharmaceuticals is recalling 418 SPAG-2 units and 808 nebulizers because some units failed to meet particle size specifications for ribavirin aerosol administration.
Shiseido America Inc. is recalling Shiseido Future Solutions LX Triple Points Bonus because the manufacturing of the active pharmaceutical ingredient did not meet GMP and quality requirements.
Ventura Foods is recalling 38 cases of Newman's Own Lite Sesame Ginger single-serve packs because a plastic foreign object was inadvertently introduced into the product stream.
Shiseido America Inc. is recalling the Future Solution LX Luxurious Eye & Lip Collection because the manufacturing of active pharmaceutical ingredients did not meet GMP and quality requirements.
AvKARE Inc. is recalling 237 cartons of Lovastatin Tablets USP, 40 mg, because annual stability testing revealed low dissolution results.
Shiseido America Inc. is recalling Future Solution LX Universal Defense SPF 50+ sunscreen because the manufacturing of active ingredient material did not meet GMP and quality requirements.
Ventura Foods is recalling Smokehouse 220 Sweet & Spicy Barbecue Sauce because a plastic foreign object was inadvertently introduced into the product stream.
Shiseido America Inc. is recalling the Future Solution LX Discovery Set because the manufacturing of active pharmaceutical ingredients did not meet GMP and quality requirements.
Ventura Foods is recalling Sysco Imperial Glazed Hot Bacon Dressing because a plastic foreign object was inadvertently introduced into the product stream.
Shionogi Inc. is recalling 968 bottles of Mefenamic Acid Capsules, 250 mg, due to the presence of black particles found during routine stability testing.
Suzuki is recalling 2017-2018 GSX-R1000 motorcycles because a gear shift error can cause the drive chain to break, leading to power loss and crash risk.
Wayfarer is recalling 2017 24 QW recreational vehicles because the installed Kidde fire extinguishers may clog or detach, potentially failing to function during a fire.
Forest River is recalling 2018 Cherokee recreational trailers because side marker lights are improperly positioned and reflectors may be missing, reducing visibility.