State
73,596 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 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2020 Escape and Transit vehicles because a defective air bag component may prevent proper inflation during a crash, increasing injury risk.
Mercedes-Benz is recalling 2019 A 220 vehicles because a poorly installed air conditioning drain hose may allow water to enter electrical components, potentially causing system malfunctions.
Ford is recalling certain 2021 F-650 and F-750 trucks because heat-protection components were not installed during assembly. Without these shields, the cabin floor and seat attachments may become too hot and cause burns.
Nissan is recalling 2020 LEAF electric vehicles because the back-up camera image may disappear while reversing, increasing crash risk.
Allison Transmission is recalling specific drive units because pressure switches may fail, potentially causing a loss of drive and increasing crash risk.
Rocky Mountain is recalling about 1,530 non-electric alloy frame Instinct and Pipeline bicycles because the front frame triangle can crack, posing fall and injury hazards.
Polaris is recalling approximately 41,200 AXYS snowmobiles because improperly secured fuel hoses may pose a fire hazard. No fires or injuries have been reported.
Blue Bird is recalling 2019-2021 Vision and All-American buses because seat belt anchorages may lack reinforcing washers, increasing injury risk in crashes.
Prodimed Plastimed Division is recalling 300 Combicath catheters nationwide due to a lack of assurance of sterility.
Prodimed Plastimed Division is recalling 180 units of Combicath Paediatric catheters nationwide because the company cannot assure the sterility of the devices.
EMD Serono is recalling 30,756 vials of Cetrotide because missing rubber stoppers could compromise sterility assurance.
Blue Bird is recalling 2018-2021 All-American and 2019-2021 Vision school buses because seat belt anchorages may lack reinforcing washers, increasing injury risk in crashes.
Verathon is recalling 437 GlideScope Core OneTouch Smart Cables because twisting during connection may damage the internal circuit board, causing video loss during critical intubation procedures.
TeDan Surgical Innovations LLC is recalling 730 sterile Phantom CS Quick Start Distraction Screws due to a lack of pouch seal.
Nutraceutical is recalling Simplers Botanicals Wintergreen Essential Oil because the packaging is not child-resistant, posing a poisoning risk.
Crate and Barrel is recalling Parke twin and full beds because the headboard can separate from the frame, posing a fall hazard.
Prodimed is recalling Combicath Paediatric catheters due to a lack of assurance of sterility. The recall covers 2,580 units distributed nationwide.
TeDan Surgical Innovations LLC is recalling 495 Phantom CS Quick Start Distraction Screws because the pouch seal is lacking, compromising the sterile labeling.
Prodimed Plastimed Division is recalling 7,220 Combicath catheters for mini bronchoalveolar lavage due to a lack of assurance of sterility.
Philips is recalling 52 EasyDiagnost Eleva DRF X-ray systems because incorrectly installed thermo switches in the main power supply may cause malfunction.
TeDan Surgical Innovations is recalling 1,965 sterile Phantom CS Distraction Screws because the packaging lacks a pouch seal, compromising the sterile claim.
TeDan Surgical Innovations LLC is recalling 340 sterile Phantom CS Quick Start Distraction Screws due to a lack of pouch seal.
TeDan Surgical Innovations LLC is recalling 3COR Distraction Screws because the pouch seal is lacking, compromising the sterile labeling.
Vitalconnect Inc. is recalling VistaSolution software due to a defect that prevented low SpO2 alerts, potentially exposing patients to short-term hypoxia.
Prodimed is recalling 1,460 Combicath catheters nationwide because the company cannot assure the products are sterile.