State
73,734 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 73,734 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Audi is recalling 2016-2018 Q3 vehicles with LED headlights because a broken front turn signal may not alert the driver, increasing crash risk.
Far East Brokers is recalling Fabulous Home Pineapple Corer & Slicers because the metal blade can detach, posing a laceration hazard.
D.B.P. Distribution is recalling Titanium 4000 capsules because they contain undeclared sildenafil and tadalafil and were marketed without an approved NDA or ANDA.
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH21A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling 434,614 endoscopic curved intraluminal staplers because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling 434,614 Straight Intraluminal Staplers (Model SDH33A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Aurora Packing Company is recalling approximately 62,112 pounds of raw beef products that may be contaminated with E. coli O157:H7. The products were shipped nationwide for further distribution and processing.
AmeriHerb International Inc is recalling 1 lb bags of dried dill weed potentially contaminated with E. coli. The product was distributed nationwide and to Canada.
Ethicon Endo-Surgery is recalling 434,614 Curved Intraluminal Staplers (Model CDH33A) because they may have an insufficient firing stroke to break the washer and form staples.
Ethicon Endo-Surgery is recalling 434,614 Endoscopic Curved Intraluminal Staplers because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery is recalling Curved Intraluminal Staplers, Model CDH25A, because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery Inc is recalling Curved Intraluminal Staplers, Model CDH21A, because they may have an insufficient firing stroke to break the washer and completely form staples.
AmeriHerb International Inc is recalling 144 lbs of Mullein leaf due to potential E. coli contamination. The product was distributed nationwide and to Canada.
Newmar is recalling 2019 Mountain Aire and Essex motorhomes because loose brake caliper mounting bolts may reduce brake effectiveness and increase crash risk.
Ethicon Endo-Surgery is recalling 434,614 Endoscopic Curved Intraluminal Staplers (Model ECS25A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery Inc is recalling 434,614 Straight Intraluminal Staplers (Model SDH25A) because they may have an insufficient firing stroke to break the washer and completely form staples.
AmeriHerb International Inc is recalling 36 lbs of Goldenseal herb due to potential contamination with generic E. coli. The product was distributed nationwide and to Canada.
Ethicon Endo-Surgery Inc is recalling 434,614 Curved Intraluminal Staplers (Model CDH29A) because they may have an insufficient firing stroke to break the washer and completely form staples.
Ethicon Endo-Surgery Inc is recalling 434,614 Model ECS33A staplers worldwide because they may have an insufficient firing stroke to break the washer and form staples.
Terumo is recalling 1,258 Electronic Patient Gas Systems because a flowmeter defect may cause inaccurate gas flow rate output.
Philips is recalling SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Abbott Ireland Diagnostics Division is recalling Alinity i Estradiol Reagent Kits because patient results may be falsely elevated for individuals treated with Mifepristone.
Philips is recalling SureSigns VS3 monitors because a software defect prevents the device from measuring, displaying, or alarming for pulse rates above 240 beats per minute.
Becton Dickinson is recalling 124 BD Veritor System Readers due to background calibration issues that may cause false positive or negative test results.