State
73,576 recalls have nationwide distribution and so reach North Dakota. 2,925 additional recalls listed North Dakota specifically in their distribution scope.
Of the 2,925 recalls naming North Dakota we have scored against our rubric, 265 (9%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 869 (30%) are Severe.
Which agencies issued them
These figures cover only the 2,925 recalls whose distribution notice names North Dakota specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
B&W Custom Truck Beds is recalling 5/8-inch stainless steel locking receiver hitch pins because the lock can be removed without a key, allowing the ball mount to detach.
Siemens is recalling 3,320 Artis angiography systems in the US because belt corrosion may cause system failure or unintended C-Arm movement.
Richelieu Foods is recalling Tuscan Garden Ranch Dressing sold at ALDI because incorrect labels failed to disclose milk and egg ingredients.
Ford is recalling 2016-2019 Explorers because roof rail covers may detach, creating a road hazard and increasing crash risk.
Triple E RV is recalling specific 2020-2021 Unity, Wonder, and Serenity models because generator fan damage to wiring may cause electrical shock.
B. Braun Medical is recalling 1,900 Filtered Triple-Leg Extension Sets because they may become occluded or unable to prime.
Luminex is recalling VERIGENE Processor SP units because they may produce false-negative results for specific enteric pathogens when used with the VERIGENE Enteric Pathogens Nucleic Acid Test Kit.
CareFusion 213, LLC is recalling ChloraPrep One-Step antiseptic applicators because fungal growth may breach package integrity. The product was distributed in the US and 12 other countries.
CareFusion 213, LLC is recalling ChloraPrep One-Step applicators due to potential fungal growth that may breach package integrity and compromise sterility.
Baxter Healthcare is recalling 408 Spectrum IQ infusion pumps because a potentially defective AC power adapter may fail over time.
DJ Orthopedics is recalling Donjoy Ultrasling Pro arm slings because a rivet at the chafe tab failed, potentially compromising the device's ability to immobilize the arm.
Clark Laboratories is recalling 80 kits of the Trinity Biotech Captia Measles IgM Kit because the positive control may run high, resulting in invalid runs and necessitating retesting.
Merits Health Products is recalling 3,054 power wheelchairs because the seat baseplate pin has broken in the field.
Datascope Corp. is recalling Cardiosave Hybrid IABP devices due to cybersecurity vulnerabilities in a TCP/IP software library that may cause loss of communication to hospital systems.
DJ Orthopedics is recalling Ultrasling Pro arm slings because a rivet at the chafe tab failed. The defect could compromise the device's ability to immobilize the arm.
CPSC is recalling Kolcraft inclined sleeper accessories due to a risk of infant suffocation. Consumers should stop using the accessory immediately and contact Kolcraft for a refund or voucher.
Peloton is recalling Tread treadmills because the touchscreen can detach and fall, posing a risk of injury to consumers.
Grace Healthcare Medical, Inc. is voluntarily recalling 35,838 compressed oxygen cylinders nationwide due to cGMP deviations. The recall was initiated in April 2021.
TJX is recalling infant sleep bags sold at T.J. Maxx, Marshalls, and Sierra because the neck opening is too large, posing a suffocation risk.
Signature Hardware is recalling Pickens Flip Up Towel Grab Bars because the towel bar can break if used for bodily support, posing fall and injury hazards.
Boston Scientific is recalling Colpassist Vaginal Positioning Devices due to potential pinholes that may compromise sterility and cause post-operative infection.
Boston Scientific is recalling Upsylon Y Mesh Kits because pinholes may breach the sterile barrier, potentially rendering the device non-sterile and causing post-operative infection.
Volkswagen is recalling 46 internal-use vehicles sold without confirmation of compliance with federal safety standards. The vehicles may have been modified and could fail to meet safety requirements.
Porsche is recalling certain 2020-2021 Cayenne models because the passenger seat heating element may not be installed, preventing proper airbag calibration and risking airbag deployment failure.
CareFusion 213, LLC is recalling ChloraPrep With Tint antiseptic applicators because fungal growth may breach package integrity at labeled storage conditions.