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A software error in the radio may prevent the rearview camera image from displaying on certain 2025–2026 Ram 1500 trucks. Without a visible rearview image, drivers have reduced visibility behind the vehicle, which increases crash risk.

Moderate·NHTSA·Sep 1, 2026

A software error in the tire pressure monitoring system (TPMS) may prevent the warning light from alerting drivers to low tire pressure. This affects certain 2024–2026 Jeep Wagoneer, Grand Cherokee, Grand Cherokee L, Grand Cherokee 4XE, Grand Wagoneer, and Cherokee models. Without this warning, drivers may not notice dangerously low tire pressure, increasing crash risk.

Moderate·NHTSA·Sep 1, 2026

Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil contains a garlic essential oil that is not approved for use in food. The product was sold in 500 ml, 250 ml, and 100 ml glass bottles between August 2025 and August 2026 at local Cincinnati retailers and online.

Moderate·FDA·Aug 31, 2026

Certain 2025–2027 Blue Bird Vision school buses have a wheelchair lift that may continue moving even when the operator tries to stop it. This happens because an electrical part can fail, leaving the lift unresponsive to controls. A moving lift with a passenger on it creates a risk of injury.

Moderate·NHTSA·Aug 31, 2026

Certain 2027 Entegra Qwest and Jayco Melbourne Prestige RVs have a taillight harness with an incorrect resistor. This may cause a false warning light to appear on the dashboard even when the taillights are working properly, which could confuse the driver or mask real safety problems.

Moderate·NHTSA·Aug 31, 2026

Certain 2026–2027 Jayco and Entegra recreational vehicles have an incorrect tire size printed on the vehicle certification label. Installing the wrong sized tires based on this label could increase the risk of a crash.

Moderate·NHTSA·Aug 31, 2026

Certain 2025–2026 Magic Tilt aluminum boat trailers have a weld defect between the winch and base plate that may cause the winch to separate during use. A detached winch could injure people nearby.

Moderate·NHTSA·Aug 28, 2026·Magic Tilt Trailers, Inc.

Certain 2027 Jayco Heartland Bighorn recreational trailers have an incorrect Gross Axle Weight Rating (GAWR) printed on the certification label. Using the wrong weight limit could lead to overloading the trailer, which increases the risk of a crash.

Moderate·NHTSA·Aug 28, 2026

Water can leak into the strobe lights on certain 2021–2023 Altec service body vehicles, causing an electrical short circuit. This short circuit can increase the risk of fire.

Moderate·NHTSA·Aug 27, 2026

Baxter is recalling one lot of Anticoagulant Sodium Citrate Solution used with apheresis devices due to potential fiberglass particles in the solution. The affected product was distributed to one customer in the United States between July 2 and July 11, 2026. No adverse events have been reported to date.

Moderate·FDA·Aug 26, 2026

American Contract Systems is recalling 2 lines of medical procedure kits and trays, 4,949 kits in total, distributed in Minnesota, Missouri, and Iowa. The recall follows Medicom's recall of specific lots of Ritmed Neurological Sponges, which may have unexpectedly variable endotoxin levels. No injuries have been reported.

Moderate·FDA·Aug 26, 20262 products

restor3d Inc. is recalling specific lots of the Veritas Standard Glenoid Baseplate used in reverse shoulder replacement surgery. A manufacturing error created incorrectly machined screw holes that may prevent peripheral screws from engaging properly during surgery. The defect affects only the standard baseplate; patient-specific baseplates are not affected.

Moderate·FDA·Aug 26, 2026

ConvaTec's Esteem Body Soft Convex Urostomy Pouches may leak from the cap during normal use. This affects multiple model numbers distributed nationwide across the U.S. No injuries have been reported to date.

Moderate·FDA·Aug 26, 2026·ConvaTec

Medtronic is recalling three MiniMed insulin pump models (640G, 670G, and 780G) that were loaned out and may have been cleaned with products that are incompatible with the pump. This could damage the case or keypad, let moisture in, and cause the pump to deliver too much or too little insulin. No injuries have been reported. The recall covers 280 affected pumps and was distributed in several European countries.

Moderate·FDA·Aug 26, 20263 products

A software defect in Beckman Coulter's DxC 500 AU Clinical Analyzer (software version 1.5 or lower) can silently overwrite customized test calculation rules when a new Parameter Package is imported. This may cause the analyzer to generate incorrect patient test results without alerting the operator to the problem. The issue only occurs when updating an existing system; newly installed systems are not affected.

Moderate·FDA·Aug 26, 2026

Paragon 28 is recalling two custom-made navicular cage foot implants because their oxygen level is above the allowed limit. Elevated oxygen may reduce the metal's ductility, meaning it may be less able to bend before breaking. The devices were distributed across the US, and no injuries have been reported.

Moderate·FDA·Aug 26, 20262 products

The Blanketrol II Model 222S thermal regulating system may experience overheating of its 115V CPU board, which can cause the device to shut down unexpectedly. This affects 182 units distributed worldwide. No injuries have been reported.

Moderate·FDA·Aug 26, 2026·Gentherm Medical

A firmware defect in the KidneyVault datalogger may cause it to lose its configuration, resulting in a blank screen and inability to display organ preservation parameters. This affects 1,445 systems distributed across the US. No injuries have been reported.

Moderate·FDA·Aug 26, 2026·Paragonix

Siemens Healthineers Immulite 2000 Systems SYP Syphilis Screen test kits may incorrectly report positive syphilis results as negative. This could allow infected patients to go undiagnosed. The affected lot codes are L2KSY2/10489085 and L2KSY6/10488319.

Moderate·FDA·Aug 26, 20262 products

Halyard LAVH PACK surgical kits (Model USAR053-11) containing Clearify Visualization System components were sterilized using ethylene oxide (EO) in a way that did not follow manufacturer instructions. This improper sterilization may have caused a kit component to leak.

Moderate·FDA·Aug 26, 2026

Boston Scientific is recalling two Suture Cinch endoscopic tissue approximation devices, the OverStitch Suture Cinch and the Suture Cinch Long. The devices may fail to deploy the cinch implant or fail to cut the suture as intended. The recall covers 60,654 units of each product, distributed in the US and many other countries. No injuries have been reported.

Moderate·FDA·Aug 26, 20262 products

The battery mounting tabs in some TD Navio Midi speech-generating devices may become damaged, allowing the battery to shift inside the device. This can cause an internal short circuit, leading to localized heating and gas venting inside the device enclosure.

Moderate·FDA·Aug 26, 2026

The ARVIS Surgical Navigation System Gen 2, a computer-controlled device used by surgeons to help position orthopedic implants during knee, hip, and shoulder surgery, has a sensor issue that can cause the image displayed through the eyepiece to appear tilted. This misalignment could affect the accuracy of surgical guidance if the surgeon relies solely on the displayed image without cross-checking with other alignment methods.

Moderate·FDA·Aug 26, 2026·Kico

The Philips Cardiac Workstation 5000 (Product Number 860439) can intermittently display inaccurate native heart rate data. This may affect the reliability of heart rate measurements used in clinical decision-making. The issue has been identified in approximately 796 units distributed worldwide.

Moderate·FDA·Aug 26, 20262 products

Intersurgical is recalling two sizes of its One-Piece Guedel Airway, a device used to keep a patient's airway open. The devices could be blocked or partly blocked, and about 22,844 units are affected. They were distributed nationwide, with US distribution in CT, FL, IN, MI, OH, and VA, and no injuries have been reported.

Moderate·FDA·Aug 26, 2026·Intersurgical2 products

Foundation Medicine's Protocol Configuration Tool (PCT) v2.0.0, used with Hamilton Microlab STAR liquid handlers to conduct F1CDx and F1LCDx tests, has a software issue that can cause the application to close unexpectedly. This affects 32 units distributed in Massachusetts and North Carolina.

Moderate·FDA·Aug 26, 2026

The EndoFLIP endoscopic measuring system has a 24-hour usage limit that causes catheters to be incorrectly marked as expired. This prevents catheters from being used in clinical procedures even though they may still be suitable for use.

Moderate·FDA·Aug 26, 2026

Spectral Instruments is recalling 75 units across two products: 40 Lago X and 35 Ami HTX. The on-screen "X-Ray On" banner can briefly be absent during the run readiness check. No injuries have been reported.

Moderate·FDA·Aug 26, 2026·Spectral Instruments2 products

Gifford's HomeMaine ice cream brand Power Play Fudge (one-quart containers) may contain small rubber pieces. The contamination was discovered during production. No injuries have been reported.

Moderate·FDA·Aug 26, 2026·HomeMaine

Grand Central Bakery's Potato Sourdough Bread products may contain metal pieces. Three varieties were affected: Potato Market Loaf (20 oz), Potato Table Loaf (20 oz), and Mini Potato Loaf (12 oz), sold in Washington on August 10, 2026.

Moderate·FDA·Aug 26, 2026·Grand Central Bakery