State
73,809 recalls have nationwide distribution and so reach Northern Mariana Islands. 23 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 23 recalls naming Northern Mariana Islands we have scored against our rubric, 0 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 18 (78%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
Entegra is recalling specific Aspire, Cornerstone, and Anthem motorhomes because front suspension ball joints may loosen and separate, potentially causing a loss of steering control.
King's Command Foods is recalling approximately 63,252 pounds of ground beef products, including meatballs and beef fritters, due to possible contamination with extraneous materials such as metal.
Nissan is recalling 2013-2014 Murano vehicles because a power steering hose clamp may fail, causing fluid leaks that could ignite near hot engine parts.
Kia is recalling 2017 Cadenza vehicles because a kinked brake vacuum hose may reduce braking performance, increasing crash risk.
Ride The Ducks is recalling 1999-2002 amphibious vehicles because headlights may be mounted too high, increasing crash risk.
Mercedes-Benz USA is recalling 2016 Smart Fortwo vehicles because the headlight adjustment mechanism may not be properly sealed, potentially allowing improper horizontal adjustment.
Physio-Control is recalling 133,330 LIFEPAK 1000 defibrillators worldwide because they may unexpectedly power off during use.