State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Skidders Footwear is recalling about 5,500 children's canvas tennis shoes because sharp rivets pose a laceration hazard. Consumers should take shoes away from children and contact the company for a refund.
Brownwood Farms is recalling Cherry Butter products because they contain milk that is not declared on the label.
Brownwood Farms is recalling Cherry Raspberry Preserves because the product contains milk that is not declared on the label.
Brownwood Farms is recalling Jalapeno Cherry Butter products because they contain milk that is not declared on the label.
Reshape Medical is recalling 114 units of the Integrated Dual Balloon System Gen 1 because distillation fluid may leak during inflation.
Roche is recalling 139 COBAS INTEGRA c111 analyzers due to a software error that may cause erroneous test results.
Brownwood Farms is recalling Pear & Cinnamon Preserves because the product contains milk that is not declared on the label.
Brownwood Farms is recalling Michigan Cherry Preserves because they contain milk that is not declared on the label.
Mercedes-Benz is recalling 672 S-Class vehicles because seat belt extenders may not retract or may break in a crash, increasing injury risk.
Brownwood Farms is recalling Strawberry Preserves because the product contains milk that is not declared on the label.
Truco Enterprises is recalling On the Border Blue Corn Tortilla Chips due to possible metal fragments in the corn flour.
Becton Dickinson is recalling specific BD Spinal Anesthesia Trays because they contain Hospira 5% Lidocaine HCI ampules that are subject to a separate recall.
Zimmer Biomet Surgical is recalling Air Dermatome II Handpiece loaners because the surface coating may blister, peel, or discolor over time. No injuries have been reported.
The FDA is recalling custom packaging for Devon Light Gloves due to added instructions for use regarding barrier integrity inspection.
Rich Products Corp is recalling specific lots of New York Style Chocolate Iced Éclairs due to the potential presence of plastic foreign material.
The FDA is recalling 118,800 units of the Covidien Devon Light Glove sub-assembly to add instructions for use regarding barrier integrity inspection.
Abbott is recalling 26,837 kits of the ARCHITECT Lactic Acid assay because the drug N-Acetyl Cysteine causes negative interference with the reagent.
The FDA is adding instructions to inspect the barrier integrity of the Covidien Devon Light Glove after application. This affects sterile surgical kits distributed in the US and abroad.
Schaerer Medical USA Inc is recalling replacement floor locking cylinders for model 7300 surgical tables because they may leak due to an incorrect O-ring.
Medimaps Group is recalling TBS iNsight v.3.0.1 software because FRAX values are incorrect when specific spine scan conditions are met.
Schaerer Medical USA Inc is recalling four 7300 model surgical tables because defective floor locking cylinders may leak due to incorrect O-rings.
Mylan Institutional, Inc. is recalling specific lots of Clonazepam Tablets, USP, 0.5 mg because they failed impurity specifications.
Mylan Institutional is recalling specific lots of Clonazepam 1.0 mg tablets because a known impurity exceeded specification limits during stability testing.
Taro Pharmaceuticals is recalling 17,100 kits of Kamedis Bio-Herbal Dandruff Care System because the active ingredient, zinc pyrithione, was found to be subpotent.
LTD Commodities and The Lakeside Collection are recalling about 39,000 projection night lights because they can short circuit, posing fire and shock risks.