Check a product

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

• 2026-10-09NHTSAAltec Industries, Inc.
  Altec Industries vehicles recalled for missing rearview camera

  Certain 2026 Altec service vehicles, aerial devices, digger derricks, and crane vehicles may have been built without a rearview camera. A missing camera reduces the driver's ability to see behind the vehicle, which can increase crash risk.

• 2026-10-09NHTSAAltec Industries, Inc.
  Altec Digger Derrick front bumper recalled for detachment risk

  Certain 2023–2024 Altec Digger Derrick vehicles have front winch bumpers secured with incorrect bolts. These bolts can fail suddenly during winch operation or cause the bumper to detach while driving, creating a road hazard and increasing injury risk.

• 2026-10-09NHTSAHyundai Motor AmericaPark Outside
  Hyundai Genesis recalled for power seat fire risk

  The front power seat motors in certain 2015–2020 Hyundai Genesis and Genesis G80 vehicles may overheat if the power seat control switch gets stuck. This overheating can cause a fire while the vehicle is parked or being driven.

• 2026-10-09NHTSA-EquipmentLippert
  Lippert power seating recalled for fire risk

  Lippert power seating assemblies have a fuse in the power cord that may not provide adequate circuit protection. If a short circuit occurs, the fuse may fail to protect the cord, increasing the risk of a fire.

• 2026-10-08FDA-PRPar Health
  Par Pharmaceutical Brevital Sodium recalled for particulate matter

  Par Pharmaceutical is recalling two lots of Brevital Sodium 500 mg/vial, an injectable anesthetic used in hospitals, because they contain tiny cellulose particles. These particles could potentially cause serious blood vessel blockages or clotting if injected. No adverse events have been reported so far.

• 2026-10-08FDA-PRGardeners Basics
  Gardeners Basics broccoli sprouting seeds recalled for Salmonella risk

  Gardeners Basics broccoli sprouting seeds may be contaminated with Salmonella, a bacteria that can cause serious illness. The contamination was identified in the seed supplier's bulk lot, which was also linked to a multistate foodborne illness outbreak. No illnesses have been reported so far.

• 2026-10-08FDA-FoodK.C. Pharmaceuticals, Inc.Class II
  PHP Animal Health Pet Drops recalled for sterility concerns

  PHP Animal Health Pet Drops lubricant eye drops may not be sterile due to a manufacturing issue. The affected products are single 15 mL bottles and twin packs distributed nationwide. No injuries have been reported.

• 2026-10-08CPSCActionary Limited, dba The Conqueror, of New Zealand
  The Conqueror Avengers medal recalled for detachable magnet hazard

  The Avengers Infinity Gauntlet medals sold through The Conqueror App contain high-powered magnets that can detach and be swallowed by children. Swallowed magnets can attract each other or metal objects, causing intestinal perforations, blockages, and serious internal injuries.

• 2026-10-08CPSCSnow Peak USA, Inc., of Portland, Oregon
  Snow Peak propane fireplace insert recalled for lava rock explosion risk

  Snow Peak's Takibi propane inserts and lava rocks can cause the rocks to ignite and explode when heated, creating a serious burn and fire hazard. The company has received one report of lava rocks exploding with minor property damage.

• 2026-10-08CPSCZhangzhou Jinhao Sen Smart Home Co., Ltd., of China
  Romorgniz six-drawer dressers recalled for tip-over risk

  Romorgniz six-drawer wooden dressers can tip over and trap children if not anchored to the wall. These dressers do not meet federal safety standards for furniture stability. About 12,078 units were sold online through Amazon between May 2025 and August 2026.

• 2026-10-08CPSCPacearth Direct, of City of Industry, California
  Pacearth swing seats recalled for fall hazard

  The metal carabiners, quick links, or webbing straps on Pacearth U-type swing seats can break during use, causing the seat to fall. The company has received at least 30 reports of falls, including nine injuries such as fractures and head trauma.

• 2026-10-08CPSCHubei Youhong Trading Co., Ltd., dba ONTHEWEI, of China
  ONTHEWEI baby bath seats recalled for drowning risk

  ONTHEWEI baby bath seats can tip over during use because they are unstable, creating a risk of drowning. The seats violate the federal safety standard for infant bath seats. About 2,140 units were sold online through Amazon between April and January 2026.

• 2026-10-08CPSCDecathlon America LLC, of San Francisco, California
  Decathlon Van Rysel GRVL AF bikes recalled for wheel dislodge risk

  The front lock nut on these gravel bicycles can loosen during use, which may cause the front wheel to dislodge or become unstable. This poses a serious crash hazard to riders. The issue affects specific Van Rysel GRVL AF models sold at REI Co-op between March 2025 and August 2026.

• 2026-10-08CPSCGenerac Power Systems Inc., of Waukesha, Wisconsin
  DR Power trimmer mowers recalled for fire and burn risk

  Grass and debris can accumulate inside DR Power Pilot and Premier trimmer mowers and ignite, creating a fire hazard. The company has received 19 reports of fires, including two minor burn injuries.

• 2026-10-08CPSCGiant Bicycle, Inc., of Newbury Park, California
  Giant SureLock LED-light bike lock keys recalled for battery risk

  LED-light keys included with certain Giant SureLock bicycle lock sets contain button batteries that children can access and swallow. Swallowing these batteries can cause serious internal injuries, chemical burns, and death. The recalled keys were sold from March 2023 through August 2026.

• 2026-10-08NHTSAHonda (American Honda Motor Co.)
  Honda CR-V and Accord Hybrid recalled for tire repair kit cap detachment

  Certain 2023–2026 Honda CR-V Hybrid, Accord Hybrid, and 2025 CR-V Fuel Cell vehicles have a tire repair kit where pressure can build inside the sealant bottle and cause the cap to detach. A loose cap can become a projectile and hit the user or bystanders.

• 2026-10-08NHTSATiffin Motorhomes, Inc.
  Tiffin Allegro Bus and Phaeton recalled for fuel leak risk

  Fuel filter hoses in certain 2022–2025 Tiffin Allegro Bus and Phaeton motorhomes may separate from their fittings, causing fuel to leak. A fuel leak near an ignition source can create a fire risk, and a sudden engine stall can lead to a crash.

• 2026-10-08NHTSASutphen Corporation
  Sutphen fire trucks recalled for fuel hose fire risk

  Certain 2021 Sutphen fire trucks equipped with Cummins L9 diesel engines may have fuel filter hoses that separate from their fittings. This can cause fuel to leak and the engine to stall, creating a risk of fire and loss of vehicle control.

• 2026-10-07FDA-PREden Brothers
  Eden Brothers Calabrese Broccoli Seeds recalled for Salmonella risk

  Eden Brothers LLC is recalling Calabrese Broccoli Seeds in multiple sizes (packets, 1-ounce, and 1-pound) because they may be contaminated with Salmonella. The affected seeds were sold online through EdenBrothers.com and Amazon.com from July through September 2026. No illnesses have been reported so far.

• 2026-10-07FDA-DeviceSiemens Healthcare Diagnostics, Inc.Class II
  Siemens Atellica CH CRP test recalled for falsely elevated results

  Siemens has recalled its Atellica CH Revised C-Reactive Protein (RCRP) test kit worldwide due to the potential for falsely elevated results. This diagnostic test is used in clinical laboratories to measure inflammation levels. Laboratories using affected lots may have received inaccurate test results.

• 2026-10-07FDA-DeviceWright Medical Technology, Inc.Class II
  Wright Medical CHARLOTTE CLAW Screws recalled for manufacturing defect

  Wright Medical manufactured CHARLOTTE CLAW Screws (REF: 40122716) with missing threads on the screwheads. These screws are designed to work with the CLAW II Polyaxial Compression Plating System for foot surgery. If used, the missing threads could prevent the screw from securing properly to the plate, potentially requiring surgery to be extended or alternative procedures performed.

• 2026-10-07FDA-DeviceKarl Storz EndoscopyClass II
  Karl Storz HOPKINS Telescope recalled for labeling error

  Karl Storz shipped HOPKINS Telescope 30° surgical visualization devices with an incorrect label on the eyepiece inside the packaging. The label error affects a small number of eyepieces (6 units) distributed in Arizona, California, and Missouri.

• 2026-10-07FDA-DeviceBeckman Coulter Mishima K.K.Class II
  Beckman Coulter AU480 analyzer recalled for software startup failure

  Certain Beckman Coulter AU480 Chemistry Analyzers may fail to start due to a software error when the system boots. When this happens, the instrument cannot begin processing patient samples, which delays test results. This affects approximately 492 units distributed worldwide.

• 2026-10-07FDA-DevicePenumbra Inc.Class II
  Penumbra RED 62 Reperfusion Catheter recalled for fracture risk

  Penumbra Inc. is recalling the Penumbra System RED 62 Reperfusion Catheter due to a manufacturing issue that may cause the catheter to fracture during use. The recall affects 43 units distributed across multiple U.S. states. No injuries have been reported to date.

• 2026-10-07FDA-DeviceTandem Diabetes Care, Inc.Class II
  Tandem t:slim app recalled for glucose monitor pairing failure

  A beta version of the Tandem t:slim iOS app (version 2.13) has a software bug that prevents it from connecting to Abbott FreeStyle Libre 3 Plus glucose monitors. Users affected by this issue cannot see their blood sugar readings in the app and cannot use automated insulin delivery; they must switch to manual pump mode instead.

• 2026-10-07FDA-DeviceOlympus Corporation of the AmericasClass II
  Olympus Tripp-Lite DisplayPort cable recalled for video dropout

  The Olympus Tripp-Lite P580-025 25ft DisplayPort Cable (Model P580-025) may cause video dropout or blackout when used with the OLYSENSE Hub System in high-power operating mode. About 543 cables were affected and distributed worldwide, including the US and Poland.

• 2026-10-07FDA-DeviceSPECTRUM MEDICAL SRLClass II2 products
  Quantum PureFlow heat exchangers recalled for blood-glycol leak risk

  Spectrum Medical is recalling two Quantum PureFlow Standard Heat Exchanger models because a leak can allow blood and glycol to mix inside the heat exchanger. The recall covers 2 products distributed across 19 states, and no injuries have been reported. No remedy has been specified yet.

• 2026-10-07FDA-DeviceMicro Therapeutics, Inc.Class II
  Micro Therapeutics Pipeline Flex device recalled for labeling mismatch

  Two units of the Micro Therapeutics Pipeline Flex Embolization Device (model PED2-300-12) were distributed with incorrect labeling. The packages were labeled as 3.00 mm diameter, but the devices inside were actually 2.50 mm diameter. This mismatch could lead to incorrect device selection during surgery.

• 2026-10-07FDA-DevicePercussionaire CorporationClass II7 products
  Percussionaire IPV ventilators recalled for anesthesia dosing risk

  Percussionaire is updating labeling for its Intrapulmonary Percussive Ventilation (IPV) devices to warn against using them with volatile anesthetic delivery systems. IPV may change how anesthetic agents are delivered, which could lead to anesthesia that is too deep or too light. This recall includes 7 products, and no injuries have been reported.

• 2026-10-07FDA-DevicePhilips North AmericaClass II12 products
  Philips Ingenia and MR systems recalled for incorrect DTI scan data

  Philips is recalling 12 MR imaging system products and related upgrades because diffusion tensor imaging (DTI) scans exported in the Enhanced MR DICOM format can contain incorrect diffusion direction data. When that export is used with third-party tractography software, the software may not be able to correctly process the data for reconstruction. No injuries have been reported.