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.
Midwest Northern Inc. is recalling 35,056 lbs of Nut Franz Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.
Midwest Northern Inc. is recalling roasted and salted pecans due to potential allergen cross-contact in the roasting oil.
Midwest Northern Inc. is recalling its Nut BBQ Blues Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.
Midwest Northern Inc. is recalling Sweet & Salty Snack Mix due to potential allergen cross-contact in the oil used to roast the nuts and seeds.
Philips is recalling 8,205 ACS-NT MRI scanners due to a potential risk of helium gas release into the examination room during a magnet quench.
Midwest Northern Inc. is recalling Asian Snack Mix due to potential allergen cross-contact in the oil used to roast nuts and seeds.
Midwest Northern Inc. is recalling Dawn's Chopped Mix, Roasted & Salted, due to potential allergen cross-contact in the roasting oil.
Midwest Northern Inc. is recalling roasted no-salt peanuts due to potential allergen cross-contact in the roasting oil.
Midwest Northern Inc. is recalling 5 lb. bags of roasted cashews due to potential allergen cross-contact in the roasting oil.
Teleflex Medical is recalling specific lots of HUDSON RCI One Way Valves because they may disconnect, causing an interruption of ventilation to patients.
Philips is recalling 295 Brilliance iCT CT systems because closing the Emergency Stop may disable the horizontal motor, allowing the couch to move during patient loading.
Mrs. Gerry's is recalling 12 lb. potato salad for undeclared imitation crab meat. Consumers with shellfish allergies should not eat the product.
AvKARE Inc. is recalling 2,135 cartons of Amantadine HCl Capsules, 100 mg, because the product failed dissolution specifications.
Datascope is recalling Mega Intra-Aortic Balloon Catheters because the U.S. Instructions for Use were missing the Contraindications section.
Swire Coca Cola is recalling 366 cases of Dr. Pepper Est. 1885 Diet, 20 FL Oz bottles due to the potential presence of foreign material.
Carefusion 2200 Inc is recalling 790 units of Jamshidi Needle Biopsy devices because the integrity of the sterile packaging is potentially compromised.
Terumo is recalling HX2 Temperature Management Systems to update cooler-heater cleaning instructions. The recall affects 2,393 units distributed worldwide.
Diamond Wipes International is recalling WipeEssentials Wet Wipes because they were manufactured with poor quality water.
GE Healthcare is recalling 43 Lunar DPX bone density systems because patient reports may be sent to hospital systems with incorrect names in the header.
Datascope is recalling 2,714 Mega Intra-Aortic Balloon Catheters because the U.S. Instructions for Use are missing the Contraindications section.
Sandoz Incorporated is recalling specific lots of Triamterene and Hydrochlorothiazide Tablets due to the presence of unrelated ingredients.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the adhesive transfer is out of specification.
GE Healthcare is recalling Lunar DPX Duo and Bravo bone density scanners because a software issue may cause reports to be filed under the wrong patient name in the hospital system.
Terumo is recalling Sarns TCM II devices to update cleaning instructions. The recall covers 2,393 units distributed worldwide.
Datascope is recalling 655 Mega Intra-Aortic Balloon Catheters because the U.S. Instructions For Use were missing the Contraindications section.