State
73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Newmar is recalling 2018-2019 Ventana and 2021 Canyon Star motorhomes because a tire valve stem extension may damage the inner wheel, risking loss of tire pressure and a crash.
Forest River is recalling certain 2018-2021 travel trailers because the breakaway safety switch may not engage the trailer brakes during separation from the tow vehicle. This defect can cause loss of vehicle control and increased crash risk.
Forest River and Coachmen motorhomes (2018-2021) are recalled for tire valve stem damage that may cause pressure loss and crash risk. Owners should seek free replacement from the manufacturer.
Honda is recalling specific tonneau covers for 2017-2020 Ridgelines because wind may cause panels to separate, creating a road hazard.
Open Book Extracts is recalling Just Hand Sanitizer because it was labeled to contain methanol.
CareFusion is recalling Alaris System PC Unit Model 8015 infusion pumps because fluid ingress can cause unresponsive or stuck keypad keys, potentially delaying or interrupting medication infusions.
CareFusion 303, Inc. is recalling BD Alaris Syringe and PCA Modules because they may display incorrect syringe types or sizes, potentially causing infusion errors.
CareFusion 303, Inc. is recalling PC Unit Front Case with Keypad Replacement Kits because fluid ingress may cause keys to become unresponsive or stuck, potentially delaying or interrupting life-sustaining infusions.
Treehouse Foods is recalling Signature Select Chewy Granola Bars because they may contain undeclared peanut butter. The recall covers 1,202 cases distributed nationwide and to Saudi Arabia.
Maquiladora Miniara S.A. de C.V. is recalling Shine & Clean Hand Sanitizer gel because FDA testing found undeclared methanol and ethanol levels below the label claim.
Open Book Extracts is recalling Always Be Clean Hand Sanitizer because it is labeled to contain methanol. The recall covers 340,000 packs distributed nationwide.
CareFusion is recalling BD Alaris infusion pumps because fluid ingress can cause unresponsive or stuck keys, potentially delaying or interrupting infusions.
Qiagen is recalling 1,474 QIAstat-Dx Respiratory SARS-CoV-2 Panel kits due to an increased rate of false positive results for Influenza A, which may lead to inappropriate antiviral use or delayed diagnosis.
RH is recalling about 270 Industrial Three-Panel Mirrors because the panels can detach and fall, posing an injury hazard. No injuries have been reported.
Kia is recalling 2020-2021 Stinger vehicles because a fuel pump defect may block fuel flow to the engine, causing loss of power while driving and increasing crash risk.
MWE Investments is recalling Westinghouse dual fuel portable generators because they can leak fuel, posing a fire and burn hazard.
Volkswagen is recalling 23 internal use vehicles, including Golf and Passat models, because they may not meet federal safety standards. Owners will be offered a repurchase.
Monoprice is recalling Category 6 Ethernet cables that do not meet flammability standards, posing a fire hazard. Consumers should stop using the cables and contact the company for a free replacement.
Kader Exports is recalling 406,080 lbs of frozen cooked shrimp from multiple brands due to possible Salmonella contamination. The product was distributed nationwide.
Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.
Teva Pharmaceuticals is recalling specific lots of Cephalexin for Oral Suspension because current Good Manufacturing Practice deviations may cause active ingredient levels to fall outside specification limits.
Talladium Inc is recalling 39 Luminesse Zirconia Discs because the linear shrinkage value on the label is incorrect and outside the acceptable range.
Hager & Meisinger is recalling 144 units of SINGLES Carbide dental burs because the US dates on the package label do not match the bar code display.
Teva Pharmaceuticals is recalling Cephalexin for Oral Suspension because test results showed the drug was below the required potency specification.
MicroPort Orthopedics is voluntarily recalling PROFEMUR Titanium and Cobalt Chrome modular necks to replace older package inserts with the most recent revision.