State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Forest River is recalling 2015-2016 Shasta Airflyte RVs because the dinette table may lack adequate support and fall, potentially causing injury.
Steve Johnson Induction Solutions is recalling specific nitrous oxide solenoid valves because end stops may break under pressure, posing an injury risk.
Forest River is recalling 2008-2016 Glaval Bus transit models because rear emergency exit labels are not placed within 16 centimeters of release mechanisms, potentially hindering quick escape.
Staples is recalling about 2,000 Back in Motion office chairs because they can tip over when leaning back, posing a fall hazard.
Academy Sports + Outdoors is recalling Outdoor Gourmet marinade injectors because small metal shavings may be present inside the product.
Fisher-Price is recalling about 34,000 infant cradle swings because the seat peg may not be fully engaged, allowing the seat to fall unexpectedly.
Vascular Solutions is recalling Guardian II Hemostasis Valves because the low-pressure seal may fail, potentially allowing air into the device and causing an air embolism.
Meditech Laboratories is recalling Formula 4 Injection vials due to incomplete data regarding production sterility.
Meditech Laboratories is recalling Formula 2 vials because an active ingredient expired before the labeled Beyond Use Date.
NutraKey, Inc. is recalling VPro Raw Plant Protein, Chocolate, because it contains undeclared soy. The recall covers 17,730 units distributed nationwide.
Whole Foods Market is recalling Maytag Blue Cheese products due to possible contamination with Listeria monocytogenes.
Actavis is recalling specific lots of amphetamine tablets because they failed impurity specifications. Consumers should stop using the product and contact their pharmacist.
Focus Diagnostics is recalling Simplexa HSV 1&2 Direct Amplification Discs because they may cause false negative or positive results and error codes.
NutraKey, Inc. is voluntarily recalling VPro Raw Plant Protein, Vanilla, due to undeclared soy. The product was distributed nationwide.
Focus Diagnostics is recalling Simplexa Group A Strep Direct Amplification Discs because they may cause false test results or error codes.
Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, potentially compromising the device's structural integrity.
Mercedes-Benz is recalling 2016 SLK300 vehicles because a backup power supply for the ignition switch may not be properly connected, creating a risk of the vehicle rolling.
Karavan is recalling 2016 KPSD trailers because a defective axle spindle flange may bend, causing excessive tire wear and increasing the risk of tire failure and a crash.
NutraKey, Inc. is voluntarily recalling VPro Raw Plant Protein nationwide due to undeclared soy, a major food allergen.
Actavis Elizabeth LLC is recalling 257,746 bottles of Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, and Amphetamine Sulfate Tablets, 20 mg, because they failed impurity specifications.
MicroAire Surgical Instruments is recalling 37 units of the PAL-R4011XL French Rasp aspiration cannula because they bent or broke during surgery.
Meditech Laboratories is recalling Formula 9 Injection vials due to incomplete production data regarding sterility assurance.
NutraKey, Inc. is recalling VPro Raw Plant Protein, Mocaccino, because it contains undeclared soy. The product was distributed nationwide.
Meditech Laboratories is recalling Formula 0 Injection due to incomplete production data regarding sterility assurance.
Meditech Laboratories is recalling Formula 2 Injection vials because one ingredient exceeded assay specifications, making the drug superpotent.