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The left-side tailgate cable on certain 2026–2027 Ford F-150, F-250 SD, F-350 SD, and F-450 SD vehicles may fail under heavy load. If the cable fails, the tailgate could drop onto the rear bumper, creating an injury risk.

Moderate·NHTSA·Oct 20, 2026

Certain 2026–2027 Ford Nautilus Hybrid and 2027 Corsair Hybrid vehicles may unexpectedly shift into neutral while driving due to corrosion in the transmission's park lock actuator circuit board. This sudden loss of drive power increases the risk of a crash.

Moderate·NHTSA·Oct 20, 2026

Certain 2022–2024 Lexus NX250, NX350, NX350 Hybrid, and NX450h+ vehicles have instrument panel displays that may fail to show engine oil pressure, coolant temperature, or electrical charge warnings. A missing warning could delay detection of engine problems and increase crash risk.

Moderate·NHTSA·Oct 20, 2026

Certain 2023–2026 Pause travel trailers were built with an incorrect connector on the 12-volt solar panel wires. A loose wire may increase the risk of fire.

Moderate·NHTSA·Oct 20, 2026

Great Dane is recalling about 840 trailers with landing gear assembly part number A30300240001. The welds on the landing gear k-brace may fail, which can cause the landing gear to collapse and increases the risk of injury. No injuries have been reported.

Moderate·NHTSA·Oct 20, 2026

Sempio Food Services, Inc. is recalling Yellow Peach canned peaches (14.10 oz cans, UPC 8801005320825, lot code 2026 06 01) because they contain elevated levels of lead. The product was distributed to Asian grocery stores across multiple states. No injuries have been reported.

Moderate·FDA·Oct 19, 2026

Right Value Drug Stores LLC is recalling compounded testosterone cypionate injection (200 mg/mL) in 5 mL and 30 mL vials due to lack of sterility assurance. The affected vials were distributed nationwide to medical offices. No injuries have been reported.

Moderate·FDA·Oct 19, 2026·Right Value Drug Stores LLC

Ashtel Studios Inc. of Ontario, California is recalling 17 fluoride toothpaste products nationwide because they were made in ways that did not meet FDA manufacturing standards. The products are sold under the Barbie, Hot Wheels, Crayola and My Little Pony names, plus the Brush Buddies, evo, ARU and BB brands. No injuries have been reported.

Moderate·FDA·Oct 19, 2026·PRITAM INTERNATIONAL PRIVATE LIMITED17 products

Certain 2026–2027 Campsite Reserve travel trailers have insufficient backer material securing the refrigerator in place. During transit, an unsecured refrigerator may move or tip over, creating a risk of injury.

Moderate·NHTSA·Oct 19, 2026

Philips Smart-hopping 2.0 AP wireless access points may experience unreliable roaming behavior when older Smart-hopping 1.0 wireless clients move between locations. This can cause loss of connection to the central monitoring system, potentially interrupting patient monitoring in healthcare facilities.

Moderate·FDA·Oct 16, 2026

Axonics has recalled certain lots of its PNE Lead Implant Kit because the 10mL luer lock syringes included in the kit may leak, break, or malfunction. This could affect the safe use of the implant procedure. The recall affects approximately 18,294 kits distributed nationwide and internationally.

Moderate·FDA·Oct 16, 2026·Axonics

Medtronic Navigation is recalling four products: certain NDI passive spheres and a biopsy needle kit. The reflective material on these items may vary, which could affect a navigation system's ability to detect and track them. No injuries have been reported.

Moderate·FDA·Oct 16, 20264 products

B. Braun Medical Inc is recalling certain SAFSITE Injection Site valves (model RV1000NC, catalog number 415068) because they may leak or allow blood to flow backward into the IV line. This could affect the safety of IV therapy. The recall affects specific lot numbers with expiration dates in September and October 2029.

Moderate·FDA·Oct 16, 2026

Think Surgical's Square Driver robotic component did not meet design specifications. This could cause the pin to become stuck or wobble during surgical drilling procedures. No injuries have been reported.

Moderate·FDA·Oct 16, 2026·Think Surgical

Abbott has updated the instructions for use for certain Amplatzer Amulet left atrial appendage occluder devices to address a risk of pulmonary artery injury during the procedure. This is a precautionary update affecting multiple model numbers across all lots and serial numbers.

Moderate·FDA·Oct 16, 2026

Broken glass was found in a piece of finished chocolate product. The recall affects 4,703 pieces of Gearharts Fine Chocolates with best-by dates from October 1, 2026 to October 21, 2026, distributed across 17 states.

Moderate·FDA·Oct 16, 2026·Gearharts Fine Chocolates

Pfizer is recalling specific lots of Levoxyl (levothyroxine sodium) 175 mcg tablets because stability testing found the drug potency fell below required specifications. This means some tablets may contain less active medication than labeled. The recall affects 134 bottles with lot number 24W07, expiring 11/30/2026.

Moderate·FDA·Oct 16, 2026·Pfizer2 products

Hepalink USA is recalling Heparin Sodium Injection (5,000 USP Units/mL) due to lack of assurance that the product is sterile. The affected multidose vials have lot number CU03232A with an expiration date of January 31, 2028. This product is used in hospitals and medical settings.

Moderate·FDA·Oct 16, 2026·Techdow

Certain lots of Telmisartan and Amlodipine 40mg/5mg tablets manufactured by Mylan Pharmaceuticals (Viatris) may contain higher-than-specified amounts of Telmisartan, the blood pressure-lowering active ingredient. The affected lots were distributed nationwide. No injuries have been reported.

Moderate·FDA·Oct 16, 2026·Viatris

Ascend Laboratories is recalling one lot of amlodipine and olmesartan medoxomil combination tablets (10mg/40mg) because they do not dissolve properly in the body. This means the medication may not work as intended. The affected lot was distributed nationwide.

Moderate·FDA·Oct 16, 2026

Wabash National is recalling certain 2027 van trailers because incorrect wheel bearing lubricant may cause the wheel end to seize. A seized wheel can lock up, which can lead to loss of vehicle handling and control and increase the risk of a crash. No injuries have been reported.

Moderate·NHTSA·Oct 16, 2026·Wabash National Corporation

Certain 2026–2027 Cedar Creek recreational trailers have a slide switch installed without proper overcurrent protection. An unprotected switch can cause the wiring to overheat, creating a fire hazard.

Moderate·NHTSA·Oct 16, 2026

Certain 2025–2027 Valor and 2026–2027 Delta recreational trailers have power seating assemblies with a fuse that may not protect adequately against short circuits. If a short circuit occurs, the inadequate protection increases the risk of fire.

Moderate·NHTSA·Oct 16, 2026·Alliance RV, LLC

Water may accumulate in the rearview camera on certain 2022–2026 Range Rover vehicles because the tailgate trim lacks sufficient drain holes. If the camera is damaged, it may stop displaying an image, reducing the driver's view behind the vehicle and increasing crash risk.

Moderate·NHTSA·Oct 15, 2026

Certain Prevost buses are missing the emergency exit operating instruction label on the entrance door. This label is required by federal safety standards and helps passengers evacuate safely in an emergency.

Moderate·NHTSA·Oct 15, 2026·Prevost Car (US) Inc.

Certain Volvo Trucks replacement sleeper cabs (VNL660 and VNL860 models) may have loose or missing structural bolts that attach the cab to the frame. If bolts are not properly secured, the sleeper cab may not protect occupants as intended during a crash.

Moderate·NHTSA·Oct 15, 2026

Intellijoint Surgical's orthopedic navigation workstations may contain a 15-inch MacBook Pro battery that is subject to an Apple recall. The battery may overheat and pose a fire safety risk during use in surgical settings.

Moderate·FDA·Oct 14, 2026

A software issue in Steris HexaVue Focus Integration System (version 2.0.18) can cause incorrect patient information to appear on manually printed surgical images. This mismatch could lead to documentation errors or clinical images being linked to the wrong patient record.

Moderate·FDA·Oct 14, 2026

LeMaitre Vascular's TufTex Over-the-Wire Embolectomy Catheter (Catalog Number E1651-88, Lot XOT00002181) failed internal testing. The balloon components can fail when exposed to pull force during use, which could compromise the device's ability to remove blood clots safely.

Moderate·FDA·Oct 14, 2026

Mindray is recalling 8 patient and telemetry monitor product lines because some operator's manuals may be insufficient or unclear about certain physiological alarm functions. The FDA classified this as a Class III recall, and no injuries have been reported. About 275,000 units are affected across the included models.

Moderate·FDA·Oct 14, 20268 products