Kansas recalls

Mays Chemical Company of Puerto Rico recalled approximately 46,315 pounds of frozen, raw pork boneless loins because they were imported into the United States without required reinspection. The pork was distributed to restaurants, institutions, and food service establishments in Puerto Rico. No illnesses have been reported.

The buckle on the cargo area bench of these e-bikes can fail to fully latch, which could allow children to fall or shift unsafely during riding. Gazelle USA has received three reports of buckles not latching properly, though no injuries have been reported yet.

Bazic Silicone Glue contains methanol but does not have child-resistant packaging required by law. The bottle is not safe from young children and could cause serious injury or death if swallowed. The label is also incorrect, falsely claiming the product is non-toxic and omitting flammability warnings.

Viofairy Hair Growth Serum bottles contain minoxidil, a medication that must be in child-resistant packaging by law. These bottles have regular caps that children can open, creating a serious poisoning risk if swallowed. The product was sold on Amazon from January 2024 through September 2025.

Certain Sunneday and Blue Bay above-ground pools have a compression strap around the outside that can create a foothold, potentially allowing children to climb into the pool unsupervised. This drowning risk exists even if the ladder is removed. No injuries have been reported.

The legs on these Hobby Lobby plush toys can detach from the body, releasing small beads inside. Young children could choke on these beads. One incident has been reported, but no injuries so far.

The fan wheel in certain NorthStar hot water pressure washers can fail, causing the burner to operate abnormally. This can produce smoke and flames during use, creating a fire hazard. The recall affects three commercial models made between January and August 2025.

These LED light sets contain coin batteries (CR2450 and CR2032) that children can easily access and swallow. Swallowing these batteries can cause serious internal burns and death. The lights also lack required safety warnings.

Mindbodygreen Ultimate Multivitamin+ bottles contain iron and are not packaged in child-resistant containers, violating federal safety requirements. Young children who swallow the contents could suffer serious injury or death from iron poisoning.

The rear wheel bolts on certain 2026 Trek FX+ and Electra Townie Go! electric bicycles can break during use, causing the rear wheel to separate from the frame. This poses a serious fall risk to riders. Trek has received seven reports of bolt breakage, though no injuries have been reported yet.

AiTuiTui Pull String Teething Toys sold on Amazon contain long string "tentacles" that children can pull off and choke on. The CPSC has received 15 reports of choking incidents and 2 reports of children biting pieces off the silicone strings. The toy does not meet federal safety standards for toys.

Sefudun 5% Minoxidil Hair Growth Serum bottles do not have child-resistant caps, as required by law. If a young child swallows the contents, it could cause serious injury or death. The product was sold on Amazon from December 2023 through August 2025.

Philips released a software update (version 4.5.0) for the Patient Information Center iX that changes how mobile event notifications are filtered. The system makes these changes without alerting users, so staff may not realize their notification settings have been altered.

The FDA identified potential cybersecurity issues with Edan's iT20 telemetry transmitter, a device used in hospitals to monitor patient heart rhythm and oxygen levels wirelessly. The company received an FDA notice asking it to address these vulnerabilities. No injuries have been reported.

The FDA identified potential cybersecurity issues with Edan iM8, iM8A, and iM8B patient monitors. These devices are used in medical settings to continuously monitor heart rhythm, blood oxygen, blood pressure, and other vital signs. The vulnerability could potentially allow unauthorized access to the device or its data.

The FDA identified potential cybersecurity issues with certain Edan M3A Vital Signs Monitors used in healthcare settings. These portable devices measure blood pressure, oxygen levels, and temperature. The FDA sent a letter to the manufacturer asking them to address the security vulnerabilities.

The FDA identified potential cybersecurity issues with Edan's M3B Vital Signs Monitor, a hospital device that tracks oxygen levels, heart rate, and CO2. Certain serial numbers manufactured between 2015 and 2024 may be affected. No patient injuries have been reported.

Edan Diagnostics' MFM-CNS and MFM-CNS Lite clinical software systems for fetal and maternal monitoring have potential cybersecurity vulnerabilities. The FDA identified these issues and requested action from the manufacturer. No patient harm has been reported.

Edan Diagnostics' MFM-CMS central monitoring system has potential cybersecurity issues that could allow unauthorized access to patient monitoring data. The FDA issued a notice asking the company to address these vulnerabilities. About 195 units are affected.

The FDA identified potential cybersecurity issues with certain Edan iX series patient monitors (models iX10, iX12, iX15). These devices are used in hospitals and clinics to continuously monitor patients' vital signs. The affected units have specific serial numbers and manufacturing dates.

Edan Diagnostics received an FDA warning letter about potential cybersecurity issues affecting certain X-series patient monitors (models X8, X10, and X12) used in hospitals and clinics. These devices continuously monitor patient vital signs, and security vulnerabilities could potentially allow unauthorized access.

The FDA identified potential cybersecurity issues with Edan's iM20 patient monitor system, which is used in hospitals and during patient transport to track vital signs like heart rhythm, blood pressure, and oxygen levels. The company received an FDA letter about these vulnerabilities. No injuries have been reported.

The FDA identified potential cybersecurity issues in Edan Diagnostics patient monitors (elite V5, V6, and V8 models). These devices are used in hospitals and clinics to continuously monitor patient vital signs like heart rate, blood pressure, and oxygen levels. The company has been notified and is working to address the vulnerabilities.

Edan patient monitors (models iM50, iM60, iM70, and iM80) have potential cybersecurity vulnerabilities that could allow unauthorized access to the device. The FDA identified these issues and is requiring the manufacturer to address them. No injuries have been reported.

Edan Diagnostics recalled certain iM3s series vital signs monitors (models iM3s, iM3As, iM3Bs, iHM3s) due to potential cybersecurity issues identified by the FDA. These monitors measure patient vital signs in clinical settings. The recall affects 136 devices with specific serial numbers distributed across the U.S. and Mexico.

The FDA identified potential cybersecurity issues with Edan's iM3 vital signs monitor, a device used in hospitals and clinics to measure blood pressure, oxygen levels, heart rate, and temperature. The company has been notified and is working to address these vulnerabilities.

The FDA identified potential cybersecurity issues with certain Edan Model M3 Vital Signs Monitors used in healthcare settings. These portable devices measure blood pressure, oxygen levels, and temperature. The company received an FDA notice about the vulnerability.

Edan Diagnostics fetal and maternal monitors (models F6, F9, F6 Express, F9 Express) may have cybersecurity vulnerabilities that could potentially allow unauthorized access to the device. The FDA identified these issues and asked the company to address them. No injuries have been reported.

The FDA identified potential cybersecurity issues with Edan Diagnostics fetal and maternal monitors (models F2 and F3). These bedside monitors are used during pregnancy and labor to track the health of pregnant women and their fetuses. The manufacturer has been notified and is working with the FDA to address the vulnerabilities.

The body support strap on certain Rifton Equipment E-Pacer gait training devices (Model K660) may fray. Fraying could potentially affect the strap's function or safety during use. The company has identified specific serial numbers affected by this issue.