State
73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wayfare Health Foods LLC is recalling Plant Based Butterscotch Pudding due to consumer complaints of package bloating, off flavors, and textural issues.
Baxter Healthcare is recalling One-Link Needle-Free IV Connectors because some units require higher-than-expected force to connect securely to standard Luer adapters.
Idelle Labs is recalling SURE 48hr Confidence Unscented Anti-Perspirant because the label lists an active ingredient that is not actually in the product.
Idelle Labs is recalling SURE 48hr Confidence Nourishing Coconut Antiperspirant & Deodorant because the label lists an active ingredient that is not actually in the product.
The Thompson's Company is recalling about 852,000 aerosol cans of WaterSeal wood and masonry protectors because leaking propellant poses a fire hazard.
Toyota is recalling approximately 1.8 million vehicles because a fuel pump failure could cause the engine to stall while driving, increasing crash risk.
Genuine Scooters is recalling 2020 Royal Alloy GT150 scooters because the front brake rotor may become uncentered, potentially causing a loss of braking and increasing crash risk.
Culinary International is recalling approximately 626 pounds of frozen chicken burritos that actually contain eggs, an undeclared allergen. No illnesses have been reported.
General Motors is recalling 2007-2008 Chevrolet Silverado and GMC Sierra trucks because front passenger air bag inflators may explode.
Forest River is recalling 2020 Shockwave Toyhauler SHT18FS-CA trailers because the Federal Placard lists incorrect tire pressure, which may increase crash risk.
Ferrari is recalling 982 vehicles because front passenger air bag inflators may explode, posing a risk of serious injury or death.
Nissan is recalling specific 2001-2011 Nissan and Infiniti vehicles because front passenger air bag inflators may explode due to propellant degradation.
Boston Warehouse Trading Corp. is recalling Holiday Travel Mugs sold at Meijer because metallic print can spark in microwaves, posing a fire hazard.
Thesaurus Global Marketing is recalling Little Bambino tricycles because lead levels in the paint and components exceed federal bans, posing a poisoning risk to young children.
Libbey Glass is recalling 33.5 oz. milk bottles that can break unexpectedly during use, posing a laceration hazard. No injuries have been reported.
The FDA is recalling Silver Bullet male enhancement capsules because they contain an undeclared active ingredient (Sildenafil) and were marketed without an approved NDA/ANDA.
KME is recalling certain 2012-2015 and 2017 Firestix Aerial Devices because swing drives may lack lubricating oil, risking gear damage and uncontrolled ladder movement.
Thoratec Corp. is recalling HeartMate 3 Mobile Power Units because excessive static electricity can cause unrecoverable power loss, potentially reducing blood flow from the left ventricular assist system.
American Health Packaging is recalling specific lots of Ranitidine Syrup because the presence of the NDMA impurity was detected in the product.
Villa Sistemi Medicali is recalling seven Apollo DRF X-ray tables because the angulation chain may fail early due to metal fatigue.
Villa Sistemi Medicali is recalling one Apollo EZ X-ray table because the angulation chain may fail early due to metal fatigue.
Roche Diabetes Care is recalling Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall affects 318,678 units distributed in the US and 35 other countries.
Carl Zeiss Meditec is recalling 151 PLEX Elite 9000 Swept-Source OCT devices because a design fault may expose operators to hazardous voltage when contacting the metal enclosure.
Roche Diabetes Care is recalling Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues that may affect device performance.
Roche Diabetes Care is recalling Accu-Chek Guide Blood Glucose Monitoring Systems due to potential power issues. The recall affects 452,392 units distributed in the US and internationally.