State
20,303 recalls have nationwide distribution and so reach North Dakota. 0 additional recalls listed North Dakota specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect North Dakota consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Cardinal Health is recalling Presource Fistulogram Packs containing recalled components including equipment drapes and table covers. Approximately 13,351 sterile packs distributed across 33 US states and Canada are affected.
Olympus THUNDERBEAT surgical instruments may have a blue seal button that remains engaged after release, potentially extending surgery time. The company is recalling 271 affected units nationwide.
The FDA is recalling Flower Orthopedics Flex-Thread TM 3.2mm Cannulated Reamer because the device can break during use, potentially requiring revision surgery.
Cardinal Health is recalling 13,351 Presource PBDS surgical procedure packs (Lot #967679) containing defective equipment drapes, table covers, and surgical room turnover kits distributed nationwide and in Canada.
Cardinal Health is recalling 13,351 surgical procedure packs containing previously recalled components including equipment drapes, table covers, and surgical room turnover kits distributed nationwide in the US and Canada.
Mazor Robotics has initiated a voluntary recall of 324 MAZOR X robotic guidance systems (Model TPL0059) due to a software issue requiring update. Affected devices were distributed nationwide in the US.
Cardinal Health is recalling 13,351 Presource PBDS surgical procedure packs distributed nationwide in the US and Canada. The specific reason for the recall was not disclosed in the available FDA notice.
BD is recalling certain lots of BACTEC Plus Aerobic/F Culture Vials because some vials have duplicate barcode sequence numbers on their labels. The recall affects 781,600 vials distributed nationwide.
LivaNova recalls 37 units of the 3T Heater Cooler System due to incorrect maintenance schedule information in the Quick Reference Guide. No injuries reported.
Cardinal Health is recalling 13,351 surgical procedure packs containing recalled components including equipment drapes, table covers, and surgical room turnover kits.
Family Health Products is recalling Crystal Clear Sodium Hydroxide sold on Amazon because the packaging is not child-resistant as required by law. The product poses a risk of chemical burns and eye irritation if accessed by children.
REV Recreation Group is recalling certain 2021-2023 Holiday Rambler and Fleetwood motorhomes due to service valve defects on LPG tanks that may cause propane leaks and fire risk. Dealers will replace valves at no cost.
Honda is recalling approximately 19 model-year 2022 Acura TLX vehicles because their tires may have sustained cuts and tears. Damaged tires can lead to loss of vehicle control and increase crash risk.
About 13,250 FORT children's play tents are being recalled because magnets used to connect pieces can come loose, posing choking and laceration risks to young children. The manufacturer is no longer in business and offers no remedy.
Gevi countertop nugget ice makers with model number GIMN-1102 and a date code before June 1, 2022, are being recalled because metal auger blades can break and create sharp metal pieces in the ice basket, posing a laceration risk. No injuries have been reported.
Chrysler recalls 2022 RAM PROMASTER vehicles with an incorrect rearview camera that cannot be installed, reducing rear visibility and increasing crash risk.
Kibbi is recalling 2022–2023 Renegade Valencia motorhomes. Service valves on LPG tanks may be improperly connected, creating a propane leak risk that could lead to fire if an ignition source is present.
YourHealthToolkit is recalling about 280 children's 5-pound weighted blankets sold on Amazon.com from January through March 2020. A young child can become entrapped inside the blanket by unzipping it, posing a risk of death by asphyxiation.
Little Sleepies is recalling approximately 450,000 Sleepyhead Loveys and Bandana Bibs because the care instruction label can detach, posing a choking hazard to young children.
Dr. Berne's MSM DROPS 5% Solution was recalled by the FDA for non-sterility issues. Lot 6786, with expiration date March 31, 2025, is distributed nationwide and internationally.
Central Admixture Pharmacy Services is recalling fentanyl-bupivacaine injectables due to lack of assurance of sterility. The recalled 250 mL bags were distributed nationwide.
Central Admixture Pharmacy Services Inc is recalling 2,664 syringes of HYDROmorphone injectable solution (30 mg/30 mL) distributed nationwide. The recall was initiated due to lack of assurance of sterility.
Olympus Corporation recalls Veran endobronchial navigation devices due to manufacturing non-conformances and insufficient electromagnetic compatibility. Approximately 6,318 units distributed worldwide are affected.
A software defect in the Philips EarlyVue VS30 Vitals Monitor prevents alarms when respiration rate limits are violated, potentially delaying detection of dangerous breathing changes. Thirteen devices distributed in Massachusetts, Michigan, and Brazil are affected.
Boston Scientific is recalling Guider Softip Guide Catheters from certain lots because the tip curve shape does not match the labeled specification. No illnesses or injuries have been reported.