State
73,503 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 73,503 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Shyft Group is recalling 2021 Utilimaster Velocity vehicles because the tire and loading placard incorrectly states a seating capacity of one instead of two.
Rossmonster is recalling 2018 Ram Promaster vans because an overtightened saddle valve bolt may damage the o-ring seal, causing a gas leak that increases fire risk.
Host Industries is recalling 2019-2021 Cascade, Rainier, Tahoe, and Mammoth trailers because a stove bolt may damage the seal, causing a gas leak and fire risk.
Forest River is recalling 2021 Wildwood and Salem trailers because red and amber clearance lamps do not reflect enough light. This visibility defect increases the risk of crashes with other vehicles.
Forest River is recalling certain 2021 IBEX travel trailers because shackle nuts may not have been properly tightened during manufacturing. Loose fasteners could fall off and cause axle detachment.
Forest River is recalling 2021 East to West Alta travel trailers because the LP/CO detector was installed in the incorrect location. This impairs propane leak and carbon monoxide detection, increasing fire and injury risks.
Certain 2021 RAM 1500 vehicles may have a rearview camera that doesn't display due to a software issue in the trailer reverse steering module. This reduces rear visibility and increases the risk of crashes.
Thor Motor Coach is recalling 2018-2022 Axis and 2018-2021 Vegas motorhomes with missing heat shields between the LP tank and chassis muffler. A missing heat shield increases fire risk; dealers will install the shield free of charge.
General Motors is recalling approximately 135,400 certain 2020-2022 Buick Encore GX and 2021-2022 Chevrolet Trailblazer vehicles because their emergency jacks can fracture if not positioned correctly, risking vehicle collapse.
BRP is recalling about 4,600 model year 2021 Can-Am Outlander and Renegade ATVs because the steering knuckle can detach from the lower arm, causing loss of control and crash risk.
FCA US is recalling 2019-2020 Ram 3500, 4500, and 5500 cab chassis vehicles because engine software may fail to warn about low oil, increasing fire risk.
Blue Star Trading is recalling about 300 Barhee Fishing Hero toy games sold on Amazon.com because metal rollers on the flying dinosaur figures contain lead levels exceeding the federal ban. Lead is toxic to young children if ingested.
GM is recalling 2021 Buick Envision vehicles—the air bag warning lamp may fail to illuminate due to a module defect. Owners should contact their dealer for a free software update.
Pfizer has recalled 139,050 vials of injectable anesthetic medications due to a label mix-up: some vials labeled as Lidocaine contain Bupivacaine, and some labeled as Bupivacaine contain Lidocaine. Patients and healthcare providers should verify medication identity before use.
Karavan is recalling 2021 Move I 1500 Long trailers because improperly welded wheel spindles can break, causing the wheel to detach and increasing crash risk.
Klein Tools non-contact voltage testers (model NCVT-1) are recalled because the on/off button can fail to disengage, causing the tester to malfunction and potentially fail to detect live voltage. One shock injury has been reported.
Pfizer is recalling 163,957 vials of 0.5% Bupivacaine Hydrochloride Injection due to a label mix-up where some vials labeled as bupivacaine may contain lidocaine, and vials labeled as lidocaine may contain bupivacaine. The mix-up could lead to patients receiving the wrong local anesthetic.
Zavation is recalling ZVplasty Direct Access Diamond Tip Trocars (11 Gauge) because some units may not be adequately sterilized. These surgical instruments are used in orthopedic and spinal procedures.
Zavation is recalling InterV CurvePlus surgical kits because products distributed as sterile may not have been adequately sterilized. 36 units were distributed nationwide.
Fujifilm's Synapse Cardiovascular software versions 6.0.4 to 6.2.1 contain a defect in the Advanced Reporting function where previously assigned patient database identification numbers can be reused for new patients when specific patient merge operations are executed.
Zavation is recalling 19 units of ZVplasty 10G FLEX KYPHOPLASTY spinal devices because distributed units may not have been adequately sterilized, posing infection risk to patients.
Zavation is recalling InterV 10G Kyphoplasty Kits because products distributed as sterile may not have been adequately sterilized. The recall affects 503 units distributed nationwide.
Zavation is recalling 130 units of 10-gauge cement delivery cannulas used in spinal procedures due to inadequate sterilization. These devices may not be sterile, creating infection risk for surgical patients.
Draeger Medical is recalling critical care ventilators due to software defects that can cause the device to restart, display incorrect oxygen alarms, and suspend weaning protocols. No patient injuries have been reported.
Zavation is recalling 58 units of 11G Direct Working Cannula Diamond Tip Mini devices (Lot 2002437) because they may not have been adequately sterilized before distribution.