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Search or scan any product against every CPSC, FDA, USDA, and NHTSA recall on record — or read the last 90 days below.

• 2026-10-19FDA-DrugPRITAM INTERNATIONAL PRIVATE LIMITEDClass II17 products
  Barbie, Hot Wheels and more toothpaste recalled for manufacturing issues

  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.

• 2026-10-19NHTSASubaru of America, Inc.Park It
  Subaru Crosstrek and Forester recalled for control arm failure

  A fastening problem in the left-front lower control arm ball joint on certain 2026 Subaru Crosstrek and Forester vehicles may cause the ball joint to separate. This can result in loss of vehicle control and increase crash risk.

• 2026-10-19NHTSAForest River, Inc.
  Forest River travel trailers recalled for refrigerator tipping risk

  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.

• 2026-10-17USDAKayemClass I
  Kayem Foods meat and poultry products recalled for temperature abuse

  Kayem Foods discovered that some of its ready-to-eat meat and poultry products may have been stored at unsafe temperatures in a warehouse cooler. The products were made between late March and early October 2026. No illnesses have been reported so far.

• 2026-10-16FDA-PRLidl US
  Gelatelli gelato recalled for Listeria monocytogenes risk

  Lidl US is recalling one lot of Gelatelli Coffee & Vanilla Gelato with Coffee Sauce & Cookie Pieces after routine quality testing found potential Listeria monocytogenes contamination. The affected product was sold at Lidl stores in Delaware, DC, Georgia, Maryland, New Jersey, New York, North Carolina, Pennsylvania, South Carolina, and Virginia between July and mid-October 2026. No illnesses have been reported.

• 2026-10-16FDA-DevicePhilips North AmericaClass II
  Philips Smart-hopping 2.0 AP recalled for connectivity loss

  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.

• 2026-10-16FDA-DeviceAxonics, Inc.Class II
  Axonics PNE Lead Implant Kit recalled for syringe defects

  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.

• 2026-10-16FDA-DeviceMedtronic Navigation, Inc.Class II4 products
  Medtronic NDI spheres and biopsy kits recalled for tracking risk

  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.

• 2026-10-16FDA-DeviceB Braun Medical IncClass II
  B. Braun SAFSITE valve recalled for leakage and backflow risk

  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.

• 2026-10-16FDA-DeviceThink Surgical, Inc.Class II
  Think Surgical Square Driver recalled for drilling defect

  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.

• 2026-10-16FDA-DeviceAbbottClass II
  Abbott Amplatzer Amulet occluder needs updated instructions

  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.

• 2026-10-16FDA-DevicePhilips Ultrasound, LLCClass I
  Philips Lumify ultrasound system recalled for connection and registration failures

  The Philips Lumify portable ultrasound system may fail to recognize previously saved transducer settings, forcing re-registration that requires Wi-Fi or cellular access—unavailable in ambulances, aircraft, or remote field settings. Additionally, the USB cable connection between the transducer and tablet/phone may become unstable or disconnect, disrupting scans. These issues could delay diagnosis or treatment.

• 2026-10-16FDA-FoodGearharts Fine Chocolates, Inc.Class II
  Gearharts Fine Chocolates recalled for broken glass

  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.

• 2026-10-16FDA-DrugPfizerClass II2 products
  Pfizer Levoxyl 175 mcg tablets recalled for reduced potency

  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.

• 2026-10-16FDA-DrugShenzhen Techdow Pharmaceutical Co., Ltd.Class II
  Hepalink Heparin Sodium Injection recalled for sterility concerns

  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.

• 2026-10-16FDA-DrugViatris, Inc.Class III
  Viatris Telmisartan/Amlodipine tablets recalled for excessive active ingredient

  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.

• 2026-10-16FDA-DrugAscend Laboratories, LLCClass II
  Ascend amlodipine/olmesartan tablets recalled for dissolution issue

  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.

• 2026-10-16NHTSAPorsche Cars North America, Inc.Park It
  Porsche 2024 911 and 718 recalled for wheel detachment risk

  The center lock wheel bolt on certain 2024 Porsche 718 Cayman GT4 RS, 911 Turbo S, 911 Turbo, 911 S/T, 911 GT3 RS, 911 GT3, 911 Carrera GTS, and 718 Spyder RS models may fracture and cause a wheel to detach. A detached wheel can cause loss of vehicle control and increase crash risk.

• 2026-10-16NHTSAForest River, Inc.
  Forest River Cedar Creek trailers recalled for fire risk

  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.

• 2026-10-16NHTSAAlliance RV, LLC
  Alliance RV recreational trailers recalled for fire risk

  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.

• 2026-10-15FDA-PRFamily Farmstead
  Family Farmstead cheddar cheese recalled for E. coli risk

  Family Farmstead Dairy is recalling Raw Mild Cheddar Cheese (lot code 7/22/27, best by date 7/22/27) because it may contain Shiga toxin-producing E. coli bacteria (strains O26:H11 and O45:H2). These bacteria can cause diarrheal illness, sometimes bloody, and in young children and elderly people can lead to a serious kidney condition called Hemolytic Uremic Syndrome (HUS). No illnesses have been reported so far.

• 2026-10-15CPSCOpal Vista Ltd., dba usOpal, of China
  usOpal Xalirium bed rails recalled for entrapment risk

  usOpal's Xalirium portable bed rails can trap users between the rail and mattress, or inside the rail frame, creating a serious risk of asphyxiation. The rails also lack required warning labels and do not meet safety standards for stability and retention straps.

• 2026-10-15CPSCPrimark US Corp., of Boston, Massachusetts
  Primark 101 Dalmatians coin purses recalled for phthalate risk

  Primark's 101 Dalmatians faux leather coin purses contain higher levels of phthalates than allowed. Phthalates can be harmful to young children, especially if ingested, and may affect development and hormones.

• 2026-10-15CPSCPapablic, Inc., doing business as Papablic, of USA, of Chicago, Illinois
  Papablic bedside sleeper recalled for suffocation and collapse risk

  Papablic convertible bedside sleepers (model PAPA03001AI) can develop serious safety problems: the mattress can shift and trap a baby between the pad and bottom, creating a suffocation hazard, and the latching mechanism can fail, causing the product to collapse. These defects violate federal safety standards for play yards.

• 2026-10-15CPSCHatsanUSA, Inc., of Bentonville, Arkansas
  Hatsan Blitz air rifles recalled for unexpected firing risk

  Hatsan Blitz and Blitz 777 air rifles can fire unexpectedly when the bolt is released before the rifle is fully cocked. This poses a risk of serious injury or death. One accidental misfire has been reported, but no injuries so far.

• 2026-10-15CPSC3M Company, of St. Paul, Minnesota
  3M Scotch thermal laminator recalled for fire hazard

  The Scotch thermal laminator model TL1302Z can overheat and catch fire. 3M has received 63 reports of the machines smoking, melting, or overheating, including 5 fires. No injuries have been reported so far.

• 2026-10-15CPSCLoving Thyself Rocks LLC, of Winter Park, Florida
  Loving Thyself Rocks crystal cups recalled for glass breakage risk

  These decorative drinking cups contain crystal stone chips between two layers of glass. The inner glass can break while the cup is in use, creating a risk of cuts or swallowing broken glass. One incident of breakage has been reported, though no injuries have occurred so far.

• 2026-10-15NHTSAShyft Group
  Shyft Spartan RV Chassis K2 recalled for fuel leak risk

  Certain 2024–2027 Spartan RV Chassis K2 vehicles have fuel filter hoses that may separate from their fittings. This can cause a fuel leak and engine stall, increasing the risk of fire or crash.

• 2026-10-15NHTSAJaguar Land Rover North America, LLC
  Land Rover Range Rover recalled for rearview camera water damage

  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.

• 2026-10-15NHTSAVolvo Trucks North America
  Volvo Trucks VNL recalled for loose structural bolts

  Certain 2025–2026 Volvo Trucks VNL cabs may have loose or missing structural bolts. These bolts are critical for cab integrity during a crash and protect the driver and passengers from injury.