State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
LeMaitre Vascular is recalling 250 units of Reddick Cholangiogram Stiffer Catheters because the latex warning symbol was not printed on the packaging.
Synergy Rx is recalling Generic VI Peel products nationwide due to a lack of assurance of sterility and CGMP deviations.
Siemens is recalling Artis Zee and Zeego fluoroscopic x-ray systems because a gap in the wireless foot switch housing could allow liquids to penetrate the interior, potentially causing the switch to fail.
Amerisource Health Services is recalling specific lots of Glipizide Extended-Release tablets because they failed to meet dissolution specifications.
LeMaitre Vascular is recalling 46 units of Reddick Scoop Tip Cholangiogram Stiffer Catheters because the latex warning symbol was missing from the packaging.
Siemens is recalling Axiom Artis fluoroscopic x-ray systems because a gap in the wireless foot switch housing could allow liquids to penetrate the interior, potentially causing the switch to fail.
Synergy Rx is recalling Hydroquinone 28% Solution because it may not be sterile. The recall covers all lots distributed nationwide.
Synergy Rx is recalling Tretinoin 0.02% in Oil Free Cream because of a lack of assurance of sterility and CGMP deviations.
Synergy Rx is recalling specific glycolic acid prescription products due to a lack of assurance of sterility and CGMP deviations.
LeMaitre Vascular is recalling Reddick Scoop Tip Cholangiogram Catheters because the latex symbol was not printed on the packaging.
Radiometer America Inc. is recalling ABL90 Flex analyzers because the 'cord blood' sample type was changed to 'cord blood arterial' and 'cord blood venous.'
LeMaitre Vascular is recalling Reddick Scoop Tip Cholangiogram Catheters because the latex warning symbol was missing from the packaging.
LeMaitre Vascular is recalling 340 Reddick Cholangiogram Stiffer Catheters because the latex symbol was not printed on the packaging.
Pharmedium Services, LLC is recalling 3,879 syringes of Buffered Lidocaine because the outer packaging is incorrectly labeled as 1% instead of 0.9%.
Colgate is recalling 14,656 bottles of PreviDent 5000 toothpaste because the rear panel is incorrectly labeled with text from a different product.
G&W Laboratories is recalling specific lots of Clindamycin Phosphate Topical Solution because an expired active ingredient was used during manufacturing.
Pfizer is recalling 582,165 vials of PROTONIX IV (pantoprazole sodium) because the drug failed potency testing at the 6-month stability time point.
KTM is recalling 2016-2017 1290 Super Duke GT motorcycles because the fuel hose can crack, potentially causing a leak and increasing fire risk.
Isuzu is recalling 2011-2017 NPR, NQR, and NRR trucks because left rear wheel bearing hub locking bolts may be loose, increasing crash risk.
Polaris is recalling about 19,200 Sportsman 850 and 1000 ATVs because heat shields can melt and exhaust springs can stretch, posing burn and fire risks.
Chrysler is recalling 2014 Fiat 500L vehicles because incorrect Powertrain Control Module software may limit engine speed and torque, increasing crash risk.
Hickory Springs is recalling specific school bus seats because a loose nut may allow the shoulder belt D-ring to detach in a crash, increasing injury risk.
REV Recreation Group is recalling 2017 Fleetwood Bounder and Holiday Rambler Vacationer RVs because Federal Placards list the wrong tire size.
Triple E RV is recalling 2017 Wonder motorhomes because a missing 'Exit' decal on the driver's door may hinder emergency egress.
BMW is recalling 2017 X5 vehicles because the passenger air bag inflator may not vent properly, potentially causing metal fragments to strike occupants in a crash.