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.
General Motors is recalling 21,567 model year 2012 Chevrolet Sonic vehicles because the transmission turbine shaft may fracture, potentially limiting speed or causing the vehicle to coast.
Hyundai is recalling 2015 Sonata vehicles because a wiring harness defect may reduce power steering assist or prevent shifting from Park, increasing crash risk.
Ford is recalling 2014 F-150 trucks because a defective steering sensor may cause total loss of steering control, increasing crash risk.
Stahl is recalling modified 2009-2014 Ford F-350, F-450, and F-550 Super Duty trucks because oil leaks from a PTO pressure switch may ignite the exhaust thermal blanket.
Big Lots is recalling Wilson and Fisher brand Cayman Resin Wicker Ottomans because the center can collapse, posing a fall hazard.
Gulf Stream is recalling 2014 Canyon Trail, Sedona, Kingsport, and Trail Master trailers because entry step rivets may fail, posing a slip and fall hazard.
General Motors is recalling 2014 Buick LaCrosse vehicles because a wiring splice may corrode, causing a missing door chime and allowing windows to operate after the vehicle is off.
Hitachi Koki is recalling two models of pneumatic nailers because they can jam and override the safety switch, posing an injury risk.
General Motors is recalling 28,789 Saab 9-3 Convertibles because the driver's seat belt retractor may break, preventing the belt from retracting properly.
Hospira is recalling 85,680 vials of Marcaine (bupivacaine HCl) injection because a customer complaint confirmed the presence of visible metal particles and discolored solution.
Golden State Medical Supply Inc. is recalling Losartan Potassium 50 mg tablets because some bottles may contain debris swept up during cleaning.
GE Healthcare is recalling Kenex ceiling suspended radiation shields and surgical lamps due to improper installation. A reported incident involved a shield falling from the ceiling.
ConMed Corporation is recalling MACROLYTE Premie Dispersive Electrodes due to confirmed complaints of sparking, no output, and burning at the cord set connection.
Toshiba is recalling two Infinix X-Ray Interventional Systems because the table may continue moving during longitudinal tilt despite error signals.
Microport Orthopedics is recalling 140 units of PATH Thread Cup Adaptors because they may be difficult to remove from the impaction handle during surgery.
Siemens Medical Solutions is recalling 345 CT systems because a rubber damper may degrade and break, potentially causing motor mounting plates to loosen and injuring operators or patients.
Cochlear Americas Inc. is recalling 288 Baha Soft Tissue Gauges due to manufacturing imperfections that could leave residual metal on patient skin.
Arrow International Inc is recalling specific Percutaneous Sheath Introducer Kits due to dilator tip damage that could cause vessel injury.
Hospira is recalling specific Plum XL and Micro Macro infusion pumps because a door roller assembly may break, preventing the cassette from locking properly.
Davol, Inc. is recalling specific lots of Bard Ventralight ST Mesh because the sterile packaging may be open or have a weak seal, potentially compromising sterility.
Philips Medical Systems is recalling IntelliSpace Portal software because SPECT reconstructions may lack scatter correction or apply resolution recovery incorrectly.
Davol, Inc. is recalling Bard Ventralight ST Mesh because the sterile inflation assembly pouch may be open or have a weak seal.
Blue Bird is recalling 2008-2013 All American school buses because a thermostat design flaw may cause a heater hose to rupture, allowing hot coolant to enter the passenger compartment.
Hospira is recalling LifeCare 5000 infusion pumps because a broken door roller pin may prevent the door from locking the cassette properly, potentially causing alarms or false occlusions.
Philips Medical Systems is recalling 6,839 CT scanners worldwide because a service latch may disengage, causing the table top to become free-floating.