State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Pastene Companies Ltd. is recalling 16 oz bags of ITAL Long Fusilli pasta because the product fails to declare the allergen wheat.
The Pastene Companies Ltd. is recalling Pastene Italian Rigatoni #31 because the semolina pasta fails to declare the allergen wheat.
The Pastene Companies Ltd. is recalling 16 oz bags of Farfalline pasta because the product fails to declare the allergen wheat.
Ford is recalling 2013-2014 Escape and C-MAX vehicles because a software error may delay side-curtain air bag deployment, increasing injury risk in rollovers.
The Pastene Companies Ltd. is recalling Pastene ITAL SPIRAL TRI COLOR pasta because it fails to declare the allergen wheat.
Fisher Scientific is recalling Fisherbrand Sterile Swabs after a customer reported the presence of an organism in a lot of wood applicator swabs.
Acumed LLC is recalling specific lots of Tension Band Pins because they were manufactured with stainless steel that does not meet specifications.
The Pastene Companies Ltd. is recalling Pastene Italian Shells #25 because the product fails to declare the allergen wheat.
The Pastene Companies Ltd. is recalling Pastene Italian Bucatini because the semolina pasta fails to declare the wheat allergen.
The Pastene Companies Ltd. is recalling Pastene ITAL NIDI #81 pasta because the product fails to declare the wheat allergen.
The Pastene Companies Ltd. is recalling Pastene Italian Ziti Rigati #20 because the semolina pasta fails to declare the allergen wheat.
Alfa Wassermann is recalling specific lots of ACE AST Reagent because they produce extremely low absorbance readings, which may affect clinical test results.
Ortho-Clinical Diagnostics is recalling VITROS Specialty Diluent because it may cause C-Reactive Protein test results to be approximately 51% lower than expected.
Caraco Pharmaceutical Laboratories is recalling 47,813 bottles of Children's Cetirizine Hydrochloride Chewable Tablets because they failed impurity testing for N-Oxide.
Siemens recalls IMMULITE Androstenedione assays because they over-recover samples above 5.5 ng/mL, contradicting the stated 10 ng/mL linearity limit.
Alfa Wassermann is recalling 731 kits of ACE ALT Reagent due to extremely low absorbance readings that may affect test accuracy.
Siemens recalls Androstenedione assays because they over-recover samples above 5.5 ng/mL, contradicting the stated 10 ng/mL limit.
Medtronic is recalling external neurostimulators because current labeling indicates the cycling feature improves device longevity and recharge interval.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products FS Diluent Pack 3 because internal testing found it may cause C-Reactive Protein test results to be approximately 51% lower than expected when used for dilution.
Caraco Pharmaceutical Laboratories is recalling 160,105 bottles of Venlafaxine Hydrochloride Extended-Release Tablets, 150 mg, because stability results showed the product did not meet drug release dissolution specifications.
Teleflex Medical is recalling 7,380 units of Dekna-lok sutures because they did not meet minimum resorption strength requirements. The affected products were distributed in the US, Ireland, and Singapore.
Baxter Healthcare Corp. is recalling 211,752 bottles of 0.9% Sodium Chloride Irrigation, USP, 1000 mL, due to the presence of nylon fibers.
Teleflex Medical is recalling CAPIO absorbable surgical sutures because they did not meet minimum resorption strength requirements. The recall affects 7,380 units distributed in the US, Ireland, and Singapore.
Teva Pharmaceuticals USA is recalling 72,356 bottles of Fluoxetine Capsules, 10 mg, due to a customer complaint trend regarding capsule odor.
Piramal Critical Care is recalling 12,600 bottles of Sevoflurane inhalation anesthetic because the product was too acidic, failing pH specifications.