South Dakota recalls
3220 federal recalls on file affecting South Dakota - 145 South Dakota-specific plus 3075 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-25FDA-DeviceOlympusClass INationwideStop using Olympus UHI-2 insufflation units
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-DeviceOlympusClass INationwideStop using Olympus insufflation unit Model UHI
Issue with software algorithm which may lead to overpressure events.
- 2026-02-25FDA-FoodWhy Not NaturalClass INationwideStop using Why Not Natural Moringa Capsules
Potential to be contaminated with Salmonella
- 2026-02-24CPSCYiruikeji2024NationwideStop using Yiruikeji2024 magnetic chess games
The recalled magnetic chess games violate the mandatory standard for toys because they contain loose magnets posing an ingestion hazard to children. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects, and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.
- 2026-02-22USDAClass INationwideThrow out Bremer frozen meatballs
Product Contamination
- 2026-02-19CPSCSamit OutdoorNationwideStop using SAMIT youth helmets immediately
The recalled helmets violate the mandatory safety standard for bicycle helmets because the helmets do not comply with the positional stability and certification requirements. The helmets can fail to protect the user in the event of a crash, posing a serious risk of injury or death due to head injury.
- 2026-02-19CPSCPrismatic 3D PrintsNationwideStop using Prismatic 3D Prints Book Nooks immediately
The recalled book nooks violate the mandatory standard for consumer products containing button cell or coin batteries because the nooks include a spare lithium coin battery that can be easily accessed by children. In addition, the spare coin battery is not in child resistant packaging, and the packaging does not have the warnings as required by Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-02-19CPSCJJGooNationwideStop using JJGoo LED balloon lights
The recalled lights violate the mandatory standard for consumer products containing button cell or coin batteries because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. Additionally, the LED lights do not have the warnings required by Reese's Law. When button cell batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2026-02-19CPSCJoly'sNationwideStop using Joly's 80% Vinegar immediately
The recalled vinegar product violates the precautionary labeling requirements under the Federal Hazardous Substances Act (FHSA) because the hazardous substance lacks required warning labels and first-aid treatment instructions. This poses a deadly risk of poisoning if the contents are swallowed and a serious injury from chemical burns to the skin and eyes if improperly handled.
- 2026-02-19CPSCHuakerNationwideStop using Huaker magnetic ball sets immediately
The recalled magnet toy building sets violate the mandatory standard for toys because they contain small balls and are intended for children under three years of age, posing a deadly choking hazard.
- 2026-02-19CPSCShenyuNationwideStop using Vive Health bed rails immediately
The recalled bed rails violate the mandatory standard for adult portable bed rails because when the bed rails are attached to a bed, users can become entrapped within the bed rail or between the bed rail and the side of the mattress, posing a serious entrapment hazard and risk of death by asphyxiation. In addition, the bed rails do not bear the required hazard warning labels.
- 2026-02-19USDAClass INationwideThrow out recalled Ajinomoto and Trader Joe's fried rice
Product Contamination
- 2026-02-18FDA-DeviceSterisClass IINationwideCheck your Steris Barco MNA adapter serial number
This is a sub-recall of event RES 96885. The supplier identified that during their manufacturing process for a limited batch of MNA-6x0 (adapter) components the incorrect configuration file was used.
- 2026-02-18FDA-DeviceSurePulse MedicalClass IIINationwideCheck Surepulse newborn heart monitor cap sizing
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
- 2026-02-18FDA-DeviceSurePulse MedicalClass IIINationwideCheck Surepulse VS Cap sizing label
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
- 2026-02-18FDA-DeviceSurePulse MedicalClass IIINationwideCheck Surepulse VS Cap Medium sizing label
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
- 2026-02-18FDA-DeviceSurePulse MedicalClass IIINationwideCheck Surepulse VS Cap Small sizing guide
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
- 2026-02-18FDA-DeviceSurePulse MedicalClass IIINationwideCheck Surepulse newborn heart monitor cap labeling
Retroactively reported; Labeling contains incorrect sizing guide for Cap, a component of the heart rate monitor.
- 2026-02-18FDA-DeviceIntuitive SurgicalClass IINationwideContact Intuitive Surgical about da Vinci 5 display firmware
Robotic-assisted surgical system has Viewer Display manufactured with outdated firmware, may result in loss of one display-loss of 3D surgical field (depth perception) but 2D maintained, or loss of both displays-complete visualization loss, without fault, instruments remain active, could lead to instrument contact with tissue, resulting in injury/bleeding; may require alternate surgical modality.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 5 M20 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 5 M12 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 7 M20 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 7 M12 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 7 B20 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 7 B12 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 3 M15 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DevicePhilipsClass IINationwideStop using affected Philips Azurion 3 M12 systems
Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active.
- 2026-02-18FDA-DeviceAlphatec SpineClass IINationwideStop using Alphatec Spine navigation osteotome
Due a design issue where the navigated array connection geometry is incorrect.
- 2026-02-18FDA-DeviceAlphatec SpineClass IINationwideStop using Alphatec ATEC Navigation Osteotome instruments
Due a design issue where the navigated array connection geometry is incorrect.
- 2026-02-18FDA-DeviceLaerdalClass IINationwideContact Laerdal about your suction unit
units manufactured in a limited time period may emit electromagnetic noise beyond the acceptable limits for RTCA application specified in RTCA DO-160G Chapter 21, Equipment Category M.
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