Product recalls in United States
Every recall and safety alert published in United States that we collect, newest first: food, vehicles, children's products, electrical goods, medicines and more.
3,853 recalls, newest first · Checked 2 minutes ago
United States2026 Freedom Aire motorhomes recall: Front chin spoiler may detach during transit
A detached spoiler may become a road hazard, increasing the risk of a crash.2026 Freedom Aire motorhomes recall: Incorrect cargo carrying capacity on Label/FMVSS 120
Incorrect weight information can allow the vehicle to be overloaded, increasing the risk of a crash.Dorman Transmission Gearshift Cables and other models recall: Detached shift cable Bushing/FMVSS 102, 114
The inability to shift into "Park" can result in a vehicle rollaway, increasing the risk of a crash.2023 Stealth and other models recall: Improperly routed coolant lines may cause a loss of drive power
A loss of drive power increases the risk of a crash.XTANT Medical Holdings, Inc recalls nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute…
Products were incorrectly labeled with a 5-year shelf life.Remel Europe Ltd. recalls Oxoid Agglutinating Sera
Affected lots are not performing to IFU criteria showing cross reactions with 2-0 within 60 seconds.Foundation Medicine, Inc. recalls Sequencing Agent SEQ0067
Possible increase in phasing, potentially resulting in false-positive BARD1 splice site indel artifact variantsUvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains two low-pressure…
In some foreseeable use conditions, the Products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety…Uvlizer c/o RAIS INTERNATIONAL LLC recalls The product is a handheld ultraviolet-C germicidal wand and contains a combination of…
In some foreseeable use conditions, the products can expose nearby persons to UVC radiation at levels significantly above limits recommended by international safety…Diversatek Healthcare recalls Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator and 3 more products
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.Davol, Inc. recalls Avitene Ultrafoam Microfibrillar Collagen Hemostat
Potential for product to contain foreign matter, confirmed to be inspect fragments.Integra LifeSciences Corp. (NeuroSciences) recalls CUSA Clarity C7000 Console
Software issue that renders the touch screen unresponsive.Foundation Medicine, Inc. recalls Protocol Configuration Tool
Potential for spontaneous closures of Hamilton HxRunControl software during execution of Autolys protocols after deployment of the PCT software for AutoLys Hamilton STAR.Beckman Coulter, Inc. recalls Access Total T4 Calibrator
Beckman Coulter has identified that Access Total T4 Calibrator lots (PN 33805) exhibit a negative bias on DxI 600/800 instruments, with slopes outside product…Micro-X Ltd. recalls Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71
X-Ray generator may malfunction resulting in the X-Ray being inoperable.Windstone Medical Packaging, Inc. recalls Custom Convenience Kits Pre Op Kit and 2 more products
The product correction was initiated because B Braun is issuing a voluntary Urgent Medical Device Correction for gravity IV administration sets as well as pump…SurgiSmoke Solutions recalls Flamingo Funnel Small and 2 more products
Certain lots of product were associated with a manufacturing nonconformance involving use of a non-gamma sterilization compatible drape.Magellan Diagnostics, Inc. recalls and 2 more products
Customers reported observing unexpectedly elevated results when using certain third-party micro-collection devices to collect capillary samples for testing with the…Arrow International, LLC recalls Arrow Echogenic Introducer Needle REF ASK-04001-BWK2 UDI code: and 7 more products
Due to receiving a notice from a supplier that the liquid adhesive were incorrectly manufactured Due to receiving a notice from a supplier that the liquid adhesive was…LSL Healthcare Inc. recalls LSL Healthcare and 5 more products
Medical procedure kits were distributed containing Webcol Large Alcohol Prep Pads which were subsequently recalled for non-sterility.Olympus Corporation of the Americas recalls OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be… and 11 more products
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.Olympus Corporation of the Americas recalls Olympus Thunderbeat II Shears w/Ultrasonic Mode and 3 more products
Potential for detachment of a distal tip component of the device during use.Medline Industries, LP recalls Medline Convenience Kits containing select SKUs of 10mL Polycarbonate Colored Syringes… and 16 more products
Unapproved design changes to the products outside of the 510(k) clearance.A little guidance
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