State
73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Homfa HPB-087 and HPB-106 cabinets are recalled because they can tip over or entrap children if not anchored to the wall.
Honda is recalling 2018-2020 Accord and 2019-2020 Insight vehicles because a software error may cause system malfunctions that increase crash risk.
Spartan Fire is recalling 2019-2021 Gladiator and MetroStar vehicles because LCD displays may lock up, potentially delaying emergency operations.
MPM Medical LLC is recalling REGENECARE HA topical anesthetic hydrogel because it was found to be contaminated with Burkholderia cepacia bacteria.
Invacare is recalling 384,767 PerfectO2 V oxygen concentrators worldwide due to a defect that may cause self-extinguishing fires or cap explosions.
CME America is recalling 4,182 NeoThrive syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.
Medtronic is recalling MiniMed 640G insulin pumps because a missing solder battery connection could interrupt power. The recall covers specific serial numbers distributed in the U.S. and abroad.
Audi is recalling 2,355 2018-2019 RS 5 Coupe vehicles because an incorrect positive battery terminal cover could prevent doors from opening or hazard lights from working after a rear crash.
CME America is recalling T34L PCA syringe pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may damage hardware.
Torrent Pharma Inc. is recalling 2,496 bottles of Anagrelide Capsules, USP 1 mg, because the product failed to meet dissolution specifications.
Medtronic is recalling 391 MiniMed 670G insulin pumps because a missing solder battery connection could interrupt power to the device.
L G Sourcing is recalling allen + roth 62-inch electric fireplaces sold at Lowe's because wiring connectors can overheat, posing a fire hazard.
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Verathon is recalling 398 BladderScan Prime Plus Probes because a change in handle material and process may cause the handle to crack.
CME America is recalling T-Syringe Pumps because motor wear may cause silent under-infusion and cleaning fluids may crack hardware.
VEO Diagnostics is recalling 15 ACCEL ELISA COVID-19 antibody test kits because the FDA removed their Emergency Use Authorization. Users should stop using the kits.
Tucson Tamale Wholesale Company is recalling Blue Corn & Veggie Tamales because plastic pieces were found in the tomato cans used to make them.
Olympus is recalling ultrasound endoscopes to update cleaning instructions and reduce the risk of patient infections.
Medtronic is recalling 206 MiniMed 630G insulin pumps due to a missing solder battery connection that could interrupt power.
CME America is recalling 4,182 T-Syringe Pumps because motor wear may cause under-infusion without alarms, and cleaning fluids may crack hardware.
Tucson Tamale Wholesale Company is recalling specific lots of Blue Corn, Veggie & Cheese Tamales because plastic pieces were found in the tomato cans used to make them.
Fiskars is recalling 16-foot extendable pole saws and pruners because the telescoping poles can separate and fall, posing a laceration hazard.
Biomeme is recalling 105 units of its SARS-CoV-2 Real-Time RT-PCR Test because the software made false positive calls due to assay issues.
Black & Decker is recalling CRAFTSMAN 10-inch corded chain saws with extension poles because they may start unexpectedly, posing a laceration risk.