Nebraska recalls

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.

Sobico USA LLC recalled approximately 13,464 pounds of frozen Siluriformes fish products (sold under the brand Shera) that were imported from Vietnam without proper U.S. import reinspection. The fish, produced June 24, 2025, were distributed to stores in Indiana, Michigan, Nebraska, New York, and Ohio. No illnesses have been reported.

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.

The labeling for the Surepulse VS Cap Large, a component of the VS Newborn Heart Rate Monitor, contains an incorrect sizing guide. This labeling error could lead to improper fit of the cap during use. No injuries have been reported.

Surepulse Medical has recalled the VS Cap Medium (part number SP-161-A1), a component of the VS Newborn Heart Rate Monitor, because the labeling contains an incorrect sizing guide. This labeling error could affect proper fit of the cap during use.

The labeling for the Surepulse VS Cap Small component of the VS Newborn Heart Rate Monitor contains an incorrect sizing guide. This affects specific lot numbers distributed in the US and several other countries. No injuries have been reported.

Surepulse Medical has recalled the VS Cap Extra Small (REF: SP-159-A1), a component of the VS Newborn Heart Rate Monitor, because the labeling includes an incorrect sizing guide. This labeling error could lead to improper cap selection for the device.

Certain da Vinci 5 Surgeon Console Viewer Displays have outdated firmware that may cause loss of the 3D surgical display or both displays entirely during surgery. When this happens, the surgical instruments remain active even though the surgeon cannot see the surgical field, which could result in unintended tissue contact, bleeding, or injury.

Philips Azurion 5 M20 X-ray imaging systems may move their patient table unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This could occur under certain conditions and pose a risk during medical procedures.

The table on certain Philips Azurion 5 M12 imaging systems may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This affects 326 units distributed worldwide, including 10 in the United States. No injuries have been reported.

Philips Azurion 7 M20 imaging systems may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This can occur under certain conditions across all software versions (R1.X, R2.X, R3.X). No injuries have been reported.

Philips medical imaging systems (Azurion 7 M12) may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This affects certain software versions across multiple model numbers. No injuries have been reported.

Philips medical imaging systems (Azurion 7 B20) may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is supposed to be engaged. This affects certain software versions across three model numbers distributed worldwide.

The examination table on certain Philips Azurion 7 B12 X-ray imaging systems may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This could pose a safety risk to patients or staff during procedures. No injuries have been reported.

Philips medical imaging tables (Azurion 3 M15 systems) may move unexpectedly when the Reset Geometry button is pressed, even if the table lock is engaged. This affects specific model numbers with software versions R1.X, R2.X, and R3.X.

The table on certain Philips Azurion 3 M12 imaging systems may move unexpectedly when the Reset Geometry button is pressed, even when the table lock is engaged. This could create a safety risk in clinical settings. Philips has identified this issue and is working on a solution.

Alphatec Spine has recalled a surgical instrument (ATEC Lateral Navigation Disc Prep Osteotome 10mm) used in spine surgery procedures. The instrument has a design defect where the connection to the Medtronic navigation tracking system does not fit correctly, which could affect its safe operation during surgery.

Alphatec Spine has recalled its ATEC Lateral Navigation Disc Prep Osteotome (10mm, model 266-01-000-10-N) used in spinal surgery due to an incorrect connection geometry in the navigated array. This defect could affect how the instrument connects to the Medtronic StealthStation navigation system during surgery. Seven units were distributed across 14 U.S. states.

Certain Laerdal Compact Suction Unit 4 RTCA models made during a specific time period may emit electromagnetic noise above acceptable levels for aircraft use. No injuries have been reported. The affected units have specific catalog numbers: 880052, 880062, or 881152.

Elekta's Leksell GammaPlan treatment planning software (versions 11.3 and 11.4) has a software error that could cause incorrect treatment location data if users do not properly update reference settings. This could result in radiation therapy being directed to the wrong location if the error goes undetected.

Elekta's Leksell GammaPlan software version 11.1 has a bug that can cause incorrect radiation targeting during Gamma Knife treatment planning. If users don't update an old reference point before creating a new treatment plan, the radiation may be aimed at the wrong location. This error may not be caught during normal review.