State
73,198 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 8 (35%) are Severe.
Which agencies issued them
These figures cover only the 23 recalls whose distribution notice names Northern Mariana Islands specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling Guider Softip Guide Catheters because certain lots were distributed with an incorrect tip curve shape that differs from labeled specifications.
Medline is recalling 106 units of Centurion Sterile CirClamp with 1.45cm bell due to kits containing an incorrect subassembly that results in incorrect bell and base size.
Central Admixture Pharmacy Services is recalling fentanyl 100 mcg/2 mL syringes due to a lack of assurance of sterility. The affected lot was distributed nationwide.
Imprimis NJOF is recalling an epinephrine-lidocaine injectable due to failed potency testing, affecting nationwide distribution. The product was compounded in April 2023 for use during eye surgery.
Central Admixture Pharmacy Services Inc is recalling 240 units of 100 mL bags of fentanyl 2500 mcg/50 mL due to lack of assurance of sterility. The product was distributed nationwide.
Central Admixture Pharmacy Services is recalling 4,550 syringes of HYDROmorphone due to lack of assurance of sterility. The product was distributed nationwide.
Dr. Berne's MSM DROPS is being recalled due to manufacturing practice deviations. The recall involves 6,060 bottles distributed nationwide and internationally.
Amerisource Health Services LLC is recalling HydrALAZINE Hydrochloride Tablets, 10 mg, nationwide due to impurities exceeding specifications in a repackaged product batch.
Dr. Berne's Whole Health Products has voluntarily recalled Dr. Berne's MSM MIST 15% Solution (30 mL bottles) due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing. The recall affects 795 bottles distributed nationwide and internationally.
Dr. Berne's MSM DROPS 5% Solution is being recalled due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall affects 3833 bottles distributed nationwide and internationally.
Zydus Pharmaceuticals recalls Oxybutynin Chloride Extended-Release Tablets 10 mg nationwide because the medication failed dissolution specifications. Affected lot numbers: M300652 and M300651.
Siemens Medical Solutions is recalling over-ear headphones used with MAGNETOM MRI systems. Lubricating grease in the headband may cause visible imaging artifacts during head examinations.
Medtronic is recalling Restore Clinician Programmer Application Software due to compatibility issues with legacy software that prevent communication with implanted neurostimulators. The recall affects 2,408 devices worldwide.
Ametek ICVS is recalling Ignition Control Module software that may cause loss of drive power or safety functions like headlights and wipers, increasing crash risk.
Platinum Driveline is recalling specific Mustang clutch covers because the material may break. Broken pieces could become projectiles, increasing the risk of injury.
Lightning eMotors is recalling 239 FT3-40, FT3-80, and FT3-120 vehicles because the instrument cluster may fail to activate brake, park, and ABS warning lights during startup.
Mercedes-Benz is recalling 2022-2023 AMG SL55 and SL63 vehicles because an improperly secured electrical wiring harness may overheat or cause a short circuit, increasing the risk of fire or loss of drive power.
Nikola is recalling 2022-2023 Tre BEV vehicles because coolant may leak inside the battery pack, creating a risk of electrical short and fire.
Transfer Flow Inc is recalling TRAX 4 Control Modules that may unexpectedly pump fuel, causing tank overflow and fire risk.
Ford is recalling certain 2020-2022 Explorer vehicles because the rear axle mounting bolt may fracture, causing the driveshaft to disconnect. This can result in loss of drive power or vehicle rollaway, increasing crash risk.
Mercedes-Benz is recalling one 2022 EQB 350 vehicle because incorrect child seat anchor covers may have been installed, potentially leading to improper child restraint installation.
KGR Distribution Corp. recalls Cocco Candy Rolling Candy in multiple flavors because the candy's rolling ball can dislodge and pose a choking hazard. One death has been reported.
CURiO Brands is recalling approximately 59,000 Capri Blue pet sprays and shampoos distributed from June through August 2023 because they can contain Pseudomonas aeruginosa bacteria, which poses a risk of serious infection to people with weakened immune systems or external medical devices.
Jayco is recalling 2024 Precept and Entegra Coach Vision XL motorhomes because their window shades may obstruct emergency exit windows. Obstructed emergency exits could delay occupant evacuation during emergencies.
Candy Dynamics is recalling approximately 70 million Slime Licker Sour Rolling Liquid Candies because the rolling ball can detach from the container, posing a choking hazard to children. Two reports of ball detachment have been received with no injuries reported.