State
73,570 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 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zavation recalls 22 ZVplasty Cement Delivery Cannulas (lot 20102490) distributed nationwide because they may not have been adequately sterilized for use in orthopedic and spinal procedures.
Vygon U.S.A. is recalling 8,320 units of its Dressing Change w/ Maxiswab kit due to improper adhesion of the sterile Tyvek lid to the tray, which could compromise the sterile barrier and potentially cause infection.
Clio LLC is recalling Clio Greek Yogurt Bar Vanilla 10-packs (UPC 861703000106) distributed nationwide due to the possible presence of metal fragments in the product.
Zavation has recalled the ZVplasty Direct Unipedicular Bone Access Kit with Drill due to potential sterilization failure. The surgical device is used in orthopedic and spinal procedures, with 11 units distributed nationwide.
Zavation's ZVplasty System surgical devices may not have been adequately sterilized, creating infection risk. The recall affects 195 units distributed nationwide in the US across multiple lot numbers.
Clio LLC is recalling Clio No Added Sugar Yogurt Bars (Mixed Berry/Peach, 50g) due to possible metal fragments in the product. Approximately 1,880 units were distributed nationwide.
Zavation is recalling ZVplasty 10G spinal implant kits that may not have been properly sterilized. The affected devices were distributed nationwide and may pose infection risk if implanted.
Clio LLC is recalling Clio Greek Yogurt Bar Vanilla/Strawberry Club pack 50g x 12, 16pc tray due to possible metal fragments in the product. Consumers should not consume the affected product.
Oxford Pharmaceuticals is recalling 6,864 bottles of Buspirone Hydrochloride Tablets, 15 mg, distributed nationwide due to the presence of foreign tablets or capsules in the product.
A cooling unit in the Philips BRILLIANCE VOLUME computed tomography system may unexpectedly eject from the gantry, posing a risk of injury. Two affected units are being recalled.
Zavation is recalling 56 units of 10 gauge direct unilateral stylets used in spinal procedures because products distributed as sterile may not have been adequately sterilized. Affected units were distributed nationwide.
Zavation is recalling 7 units of 11G DIRECT SINGLE spinal implants (lots 2001185 and 2001243) because products distributed as sterile may not have been adequately sterilized. The devices were distributed nationwide.
Zavation's 10G Direct Single Bone Access Kits are being recalled because products distributed as sterile may not have been adequately sterilized, posing infection risk in orthopedic procedures.
A software defect in Change Healthcare Enterprise Viewer versions 2.0 and 2.1 prevents the display of image presentation styles. The viewer is used nationwide for displaying medical images.
K2M, Inc is recalling Cascadia AN Interbody Convex lumbar implants with mislabeled product dimensions. The affected sizes include 10x22x14mm, 10x28x14mm, and 10x22x15mm. No injuries have been reported.
Boehringer Ingelheim Pharmaceuticals is recalling Micardis 80 mg tablets (Lot #860412, expiration September 2022) because the tablets contain less active ingredient than required. This is a voluntary Class II recall.
Mylan Institutional LLC is recalling Thiamine Hydrochloride Injection USP 200 mg/2 mL due to vials labeled with incorrect lot numbers. The cartons contain the correct lot number 200906 but vials inside are labeled with lot number 200901.
Jaguar Land Rover is recalling 2020-2022 Defender X vehicles with smoked rear lights because a voltage spike can cause turn signals and brake lights to fail.
One More Auto Parts is recalling Lasfit headlight bulbs that are too bright during the first ten minutes of use, posing a crash risk.
Coach House is recalling 2021 Platinum vehicles because an overtightened bolt on the cooking stove may damage the seal, causing a gas leak that increases fire risk.
Honda is recalling 2022 Odyssey vehicles because second-row outboard seat frames have deformed locking mechanisms that may prevent them from locking into place. Unlocked seats could move unexpectedly, increasing injury risk.
Highland Ridge RV is recalling certain 2019-2021 fifth wheel and travel trailers because a propane regulator may fail, increasing fire risk.
KZRV is recalling 2018-2019 Sidewinder RVs because a propane regulator may fail, increasing pressure and fire risk.
Jayco is recalling approximately 87,649 certain 2017-2021 travel trailers and fifth wheels with defective Winntec propane regulators that may fail and increase fire risk.
Starcraft RV is recalling specific 2017-2021 travel trailers and fifth wheels because a propane regulator may fail, increasing fire risk.