South Dakota recalls

Olympus Corporation is removing Thunderbeat 5mm pistol grip surgical instruments (Model TB-0535PC) from the market worldwide due to ongoing reports of adverse events during use. No specific injuries have been reported, but the company is taking action out of caution.

Olympus Corporation is removing Olympus Thunderbeat 5 mm, 45 cm pistol grip surgical instruments (Model TB-0545PC) from the market due to ongoing reports of adverse events during use. This Class II recall affects approximately 30 units distributed worldwide, including the United States, Brazil, Canada, Germany, Mexico, and Japan.

Olympus Corporation is recalling the Thunderbeat 5 mm, 20 cm front-actuated grip surgical instrument due to continued reports of adverse events during use. The recall affects all lots of this model worldwide, including the US and several other countries.

Olympus is removing the Thunderbeat 5 mm, 35 cm, Front-Actuated Grip surgical instrument (Model TB-0535FC) from distribution due to ongoing reports of adverse events during use. The device has been distributed worldwide, including across the US and several other countries.

Olympus is recalling the Thunderbeat 5 mm, 45 cm Front-Actuated Grip surgical instrument (Model TB-0545FC) worldwide due to continued reports of adverse events during use. The company has determined that removal of this device from the market is necessary.

Olympus Corporation is removing Thunderbeat 5 mm, 20 cm surgical instruments (Model TB-0520FCS) from the market due to ongoing reports of adverse events during use. The company has identified a safety concern affecting all lots of this device.

Olympus is recalling its Thunderbeat 5 mm, 35 cm Front-Actuated Grip Type S surgical instruments (Model TB-0535FCS) due to ongoing reports of adverse events. The recall affects 88,268 units distributed worldwide, including in the United States, Brazil, Canada, Germany, Mexico, and Japan.

Olympus Corporation is removing the Thunderbeat 5 mm, 45 cm Front-Actuated Grip Type S surgical instrument from use worldwide due to ongoing reports of adverse events during use. This affects approximately 9,542 units across the US and several other countries.

Medica Corporation's capillary tubes used with EasyBloodGas and EasyStat devices are giving false potassium results—up to 20% higher than actual levels. This could lead doctors to misinterpret a patient's potassium levels and provide incorrect treatment.

Immunotech's Estrone RIA diagnostic kit may rarely produce falsely high hormone test results in patients. This could potentially lead to unnecessary or incorrect medical decisions. The issue affects only specific lot numbers and occurs very infrequently.

Bard Peripheral Vascular is recalling multiple central venous catheter trays and kits because the outer packaging may be damaged, which could compromise the sterile barrier that protects the medical device. The recall affects several Broviac and Hickman catheter products with specific lot numbers manufactured between April 2028 and August 2030.

Medline Industries is recalling 23 models of IV administration and extension sets because the male connectors may leak, crack, or break during use under certain conditions. This could cause delays in treatment, blood loss, infection, air embolism, or patients not receiving the correct medication dose.

CVS Private Label wound care gel (model CVS405406) may have packaging defects that could compromise the sterile barrier protecting the product. This affects specific lot numbers and could allow contamination of the gel used for minor burns, cuts, and abrasions.

Integra LifeSciences has recalled certain lots of MEDIHONEY Calcium Alginate dressing due to potential packaging failures that could compromise the sterile barrier. If the sterile seal is broken, the wound dressing may become contaminated before use. This affects three model numbers distributed worldwide, including to healthcare facilities in the US and internationally.

Integra LifeSciences is recalling specific batches of MediHoney Gel wound dressing because the sterile packaging may fail, potentially allowing contamination. This affects models 31805 and 31815 distributed worldwide. No injuries have been reported.

Olympus has recalled the High Flow Insufflation Unit Model UHI-3 due to a software algorithm issue that can cause overpressure events during abdominal cavity insufflation procedures. This medical device is used in laparoscopic surgery to maintain proper pressure and clear the surgical field. No injuries have been reported.

Olympus has recalled its High Flow Insufflation Unit (Model UHI-2) used during abdominal surgery because a software problem may cause the device to create excessive pressure in the abdominal cavity. The issue affects all 744 units distributed nationwide. No injuries have been reported.

Olympus Corporation is recalling the High Flow Insufflation Unit (Model UHI) used during abdominal surgery due to a software problem that may cause overpressure events. The device is used to inflate the abdominal cavity and remove smoke during laparoscopic surgery. No injuries have been reported.

Why Not Natural Moringa Capsules (lot #A25G051, expiration 07/2028) may be contaminated with Salmonella, a bacteria that can cause serious illness. The affected capsules were distributed nationwide. No illnesses have been reported so far.

These magnetic chess games contain loose magnets that children can swallow. When swallowed, high-powered magnets can stick together inside the digestive system and cause serious injury or death, including intestinal perforation, twisting, blockage, and blood poisoning.

Rosina Food Products recalled approximately 9,462 pounds of Bremer brand frozen Italian-style meatballs sold at Aldi due to possible metal fragments in the product. The affected packages are 32-oz. bags with a "BEST BY" date of 10/30/26, produced on July 30, 2025. No injuries have been reported so far.

SAMIT youth helmets sold on Amazon fail to meet safety standards for bicycle helmets. In a crash, these helmets may not protect your child's head, risking serious injury or death. The helmets don't meet required stability and certification standards.

Prismatic 3D Prints Book Nooks contain a spare coin battery (CR2032) that children can easily access and swallow. The battery is not in child-resistant packaging and lacks required safety warnings. Swallowing these batteries can cause serious internal injuries, chemical burns, and death.

JJGoo LED balloon lights contain button cell batteries that children can easily access and swallow. Swallowing these small batteries can cause serious internal injuries, chemical burns, and death. The lights also lack required safety warnings.

Joly's 80% Vinegar sold on Amazon is missing required warning labels and safety instructions. The product can cause serious poisoning if swallowed or chemical burns if it contacts skin or eyes. About 450 bottles were sold between May and November 2025.

Huaker magnetic toy building sets sold on Amazon contain small balls that pose a serious choking hazard for children under 3 years old. These sets violate federal toy safety standards. About 782 sets were sold between September and November 2025.

Vive Health bed rails (models LVA1024 and LVA3031BLK) can trap users between the rail and mattress, creating a serious risk of entrapment and death by asphyxiation. The rails also lack required warning labels. About 12,355 units were sold online from August 2023 through December 2025.

Ajinomoto Foods North America is recalling frozen chicken fried rice products that may contain glass. The recall affects Ajinomoto Yakitori Chicken Fried Rice and Trader Joe's Chicken Fried Rice with specific best-by or best-before dates. The company discovered the problem after receiving four reports of glass found in the product, though no injuries have been confirmed.

Steris Corporation identified that a limited batch of MNA-6x0 adapter components used in the Barco MNA with HexaVue IP Integration System were manufactured with an incorrect configuration file. This affects 10 units with specific serial numbers distributed across seven states.

Surepulse Medical has recalled the VS Cap Extra Large component used in their VS Newborn Heart Rate Monitor because the labeling includes an incorrect sizing guide. This could lead to improper fit of the cap on the monitor. No injuries have been reported.