State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Valor Athletics is recalling 100 Olympic weight benches because a weld can break, posing an injury risk. No injuries have been reported.
Gourmet Kitchen, Inc. is recalling 394 boxes of Spicy Shrimp Chopsticks because the products may contain peanut protein.
Hewitt is recalling about 1,700 chain-driven marine winches because the roller chains can break, posing an injury risk to users and bystanders.
Gourmet Kitchen, Inc. is recalling Lobster Spring Rolls because they may contain peanut protein. The recall covers 42 boxes distributed nationwide.
Philips Medical Systems is recalling 918 ADAC Vertex Gamma Cameras because detector heads may drift and contact patients during imaging.
Forest River is recalling 2014-2016 Vengeance trailers because incorrect certification labels may cause operators to overload the vehicle, increasing crash risk.
Gourmet Kitchen, Inc. is recalling Shrimp Maui products because they may contain peanut protein. The recall covers 135 boxes distributed nationwide.
Gourmet Kitchen, Inc. is recalling Asparagus Roll Ups because the products may contain peanut protein. The recall covers 315 cases distributed nationwide.
Gourmet Kitchen, Inc. is recalling Spinach & Goat Cheese Focaccia because the product may contain peanut protein, posing a risk to individuals with peanut allergies.
Electrolux is recalling Kenmore Elite slide-in ranges sold at Sears because a sharp edge on the stainless steel trim below the control panel can cause cuts.
Electrolux is recalling about 250 Kenmore Elite dual fuel ranges sold at Sears because the burner flame can go out while gas is on, posing fire and burn risks.
Gourmet Kitchen, Inc. is recalling Lobster & Shrimp Spring Rolls because they may contain peanut protein. The recall covers 120 boxes distributed nationwide.
Natural Foodworks Group is recalling Purely Elizabeth Cranberry Cashew Ancient Grain Muesli because it contains undeclared sulfur dioxide.
Alvogen, Inc. is recalling Nitrofurantoin Monohydrate/Macrocrystalline capsules because they failed a dissolution specification test.
Akorn, Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim Oral Suspension because the sulfamethoxazole failed to meet dissolution specifications.
Synthes, Inc. is recalling 8,175 TFNA Proximal Femoral Nails because the locking mechanism was assembled too close to the top, potentially causing surgical delays.
Akorn, Inc. is recalling specific lots of Sulfamethoxazole and Trimethoprim Oral Suspension because the sulfamethoxazole component failed to meet dissolution specifications.
BioHorizons is recalling 48 units of the Tapered HD Upgrade Set because they were packaged with a stainless steel drill instead of the correct titanium component.
Apotex Inc. is voluntarily recalling 6,467 units of Olanzapine 10 mg orally disintegrating tablets because the drug is subpotent.
Philips Medical Systems is recalling 975 nuclear gamma cameras because the collimator exchange carriage and storage cabinet were misaligned.
Akorn, Inc. is recalling 8,400 cups of Sulfamethoxazole and Trimethoprim oral suspension because the sulfamethoxazole failed to meet dissolution specifications.
Mission Pharmacal is recalling 1,992 kits of Sodium Sulfacetamide 9% and Sulfur 4.5% Wash due to microbial contamination.
Fujifilm Medical Systems is recalling Synapse Cardiovascular software versions v4.0.8 and v4.0.8 SR1 because patient demographics in exported reports may not match the clinical reports.
Stryker Howmedica Osteonics is recalling four 80 mm Kinemax Stem Extenders because they were shipped in boxes labeled for the 80 mm part but contained 40 mm extenders.
Cipla Limited is recalling 140,625 vials of Levalbuterol Inhalation Solution because the product failed impurity specifications. The affected lot is distributed nationwide.