State
72,919 recalls have nationwide distribution and so reach Northern Mariana Islands. 22 additional recalls listed Northern Mariana Islands specifically in their distribution scope.
Of the 22 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 8 (36%) are Severe.
Which agencies issued them
These figures cover only the 22 recalls whose distribution notice names Northern Mariana Islands specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Honda is recalling certain 2023-2025 CMX300, CMX500 and CL500 motorcycles because the handlebar lock screw may loosen and detach, potentially interfering with steering.
Gillig is recalling 2023-2026 Low Floor transit buses because a splice in the high voltage cable reduces amp capacity, increasing the risk of overheating and fire.
Kluster Fun Tabletop Magnet Chess Games are being recalled because they contain loose high-powered magnets that fit within CPSC's small parts cylinder, posing an ingestion hazard to children.
17 Stories Furniture 14-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards. They violate the STURDY Act.
LFTE USA is recalling Playground Swing Set Seats with model number 999604 because the rivets used to support the swing seat can fail, posing a fall hazard to children.
LIVEHOM 11-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards. They violate the STURDY Act.
ProRider bicycle helmets are being recalled because they do not comply with the mandatory safety standard for impact attenuation, positional stability, labeling and certification.
Abiomed is recalling the Impella RP with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Abiomed is recalling the Impella RP, product code 0046-0011, because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Abiomed is recalling the Impella RP Flex with SmartAssist because the differential pressure sensor may malfunction, causing sensor values to drift. The FDA has classified this recall as Class I.
Aluminum Trailer Company is recalling certain 2023-2026 PL700 and PL750 recreational trailers because the generator exhaust is vented directly under the slide-out bedroom, letting carbon monoxide enter the cabin.
123Herbals is recalling Silintan 25-count pill bottles because FDA analysis revealed the presence of undeclared meloxicam. The FDA has classified this recall as Class I.
Mojo Max Fusion XXX capsules are being recalled because FDA analysis revealed undeclared sildenafil at 13.1 mg per capsule and tadalafil at 13.8 mg per capsule. The FDA has classified this recall as Class I.
Teva Pharmaceuticals is recalling three lots of Metoprolol Succinate Extended-Release Tablets 200 mg after the product failed dissolution specifications.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 50 mg after the product failed dissolution specifications.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 25 mg after the product failed dissolution specifications.
Olympus is recalling the ShockPulse-SE Lithotripsy System Generator after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
B. Braun Medical is recalling 21G x 4.4 cm Winged Infusion devices, model 7B3050, because the needle tip may be dull or blunt, difficult to advance, or may break.
Teva Pharmaceuticals is recalling six lots of Metoprolol Succinate Extended-Release Tablets 100 mg after the product failed dissolution specifications.
GE Healthcare is recalling Centricity Universal Viewer Zero Footprint Client because under certain workflows the patient information shown may not match the images displayed.
Olympus is recalling ShockPulse-SE Lithotripsy System reusable probes after further instances of the generator remaining in a blinking phase waiting to recognize the transducer.
B. Braun Medical is recalling 21GA Winged Infusion Sets, model 7M2802, because the needle tip may be dull or blunt, difficult to advance, or may break.
Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-1218, because of the potential for rubber fragment detachment during use.
Esaote is recalling five Endocavity ultrasonic probes, model E 3-12, because a potential weakness in the probe body may allow liquid to leak from the casing near the cable.
Roche is recalling cobas pro sample supply units on software versions before 03-02 because a defect can make the analyzer repeat the last calculated result for all later measurements.