Browse the most recent U.S. safety recalls in our connected official government data.
3,525 recalls in our current data. Showing 3,001–3,100, newest first.
A bolt that loosens or breaks during vehicle operation can result in loss of vehicle control, increasing the risk of a crash.
Company / brand: General Motors recalls
Official ID 26V304000 · Official record ↗
The electronic start/stop button on the pressure washer can malfunction and self-start, posing a risk of serious injury or death due to carbon monoxide poisoning, if the unit is in…
Company / brand: Generac Power Systems recalls
Official ID 26494 · Official notice ↗
The recalled tower stools can collapse or tip over while in use, and a child's torso can fit through the openings on the front and back sides, posing a risk of serious injury and d…
Company / brand: SuzhouGongYeYuanQu Wan Yi Shen Jia MaoYiShangHang dba Cosyland Official recalls
Official ID 26493 · Official notice ↗
The platform inside the recalled tower can loosen over time, causing it to become unstable or detach, and ultimately posing a fall hazard to young children.
Company / brand: Guidecraft recalls
Official ID 26490 · Official notice ↗
The kettle's handle can loosen and separate from the kettle, causing hot contents to spill, posing a risk of serious injury due to a burn hazard.
Company / brand: ZWILLING J.A. Henckels Aktiengesellschaft recalls
Official ID 26489 · Official notice ↗
The recalled harness' D-ring can release, allowing the attachment point to open, posing a risk of serious injury or death from a fall hazard.
Company / brand: Petzl America recalls
Official ID 26488 · Official notice ↗
The recalled harnesses are missing rivets in the FAST LT PIN-LOCK buckles, causing the buckles to open, posing a risk of serious injury or death from a fall hazard.
Company / brand: Petzl America recalls
Official ID 26487 · Official notice ↗
The weight plates can fail to engage completely during weight adjustment and dislodge from the dumbbell handle when used, posing an impact hazard.
Company / brand: Amazon.com Services recalls
Official ID 26486 · Official notice ↗
The swing seat can detach from the frame while in use, posing a risk of serious injury or death from a fall hazard.
Company / brand: Costco Wholesale recalls
Official ID 26485 · Official notice ↗
The recalled coin batteries are not in child-resistant packaging and do not bear the warning labels required under?Reese's Law.?When button cell or coin batteries are swallowed, th…
Company / brand: Guangzhou Lichengbei Battery Technology Co recalls
Official ID 26484 · Official notice ↗
The Misco Sports Badminton Toy Sets violate the mandatory safety standard for children's toys because the shuttlecocks contain button cell batteries that can be easily accessed by …
Company / brand: Missry Associates recalls
Official ID 26483 · Official notice ↗
The ATV's speed limiter control can malfunction, causing unexpected speed and acceleration, posing a serious risk of injury or death from crash hazard.
Company / brand: BRP US recalls
Official ID 26482 · Official notice ↗
The recalled teething toys violate the mandatory standard for toys because the silicone strings are smaller and longer than permitted. The silicone strings can reach the back of th…
Company / brand: Zhongwan Guangzhou Technology Co recalls
Official ID 26481 · Official notice ↗
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment and drowning hazards to swimmer…
Company / brand: Shenzhen Jiangtou Technology Co recalls
Official ID 26480 · Official notice ↗
The recalled light fixture's frame can detach from the pendant downrod during installation, posing a risk of serious injury or death from an impact hazard.
Company / brand: Minka Lighting Group recalls
Official ID 26479 · Official notice ↗
A loss of drive power increases the risk of a crash.
Company / brand: Lucid Usa recalls
Official ID 26V309000 · Official record ↗
A loss of exterior lights can reduce the visibility of the vehicle to other drivers, increasing the risk of a crash. Inoperative equipment can delay emergency response, increasing …
Company / brand: Hale Products recalls
Official ID 26E030000 · Official record ↗
A liftgate that falls unexpectedly increases the risk of injury.
Company / brand: Hiab Usa recalls
Official ID 26E029000 · Official record ↗
Resorbable bone void filler falls outside standard specifications.
Company / brand: Orthorebirth Co recalls
Official ID Z-2132-2026 · Official record ↗
Resorbable bone void filler falls outside standard specifications.
Company / brand: Orthorebirth Co recalls
Official ID Z-2131-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2130-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2129-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2128-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2127-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2126-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2125-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2124-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2123-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2122-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2121-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2120-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2119-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2118-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2117-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2116-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2115-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2114-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2113-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2112-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2111-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2110-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2109-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2108-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2107-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2106-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2105-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2104-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2103-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2102-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2101-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2100-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2099-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2098-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2097-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2096-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2095-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2094-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2093-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2092-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2091-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2090-2026 · Official record ↗
Medline has identified issues related to calibration of the equipment used to sterilize and package the devices. All products were exposed to the validated sterilization and packag…
Company / brand: Medline Industries recalls
Official ID Z-2089-2026 · Official record ↗
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2088-2026 · Official record ↗
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2087-2026 · Official record ↗
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2086-2026 · Official record ↗
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2085-2026 · Official record ↗
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2084-2026 · Official record ↗
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2083-2026 · Official record ↗
The devices were distributed without required FDA premarket clearance or approval.
Company / brand: DFI Co recalls
Official ID Z-2082-2026 · Official record ↗
Respiratory/sore throat panel test may result in false negative results and control failures.
Company / brand: BioFire Diagnostics recalls
Official ID Z-2081-2026 · Official record ↗
Ophthalmic Tissue Forceps (DEX") are sterile, hand-held ophthalmic surgical instruments designed for grasping, manipulating, compressing, pulling, or joining eye and/or surrounding…
Company / brand: Katalyst Surgical recalls
Official ID Z-2080-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2079-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2078-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2077-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2076-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2075-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2074-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2073-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2072-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2071-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2070-2026 · Official record ↗
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Company / brand: Katalyst Surgical recalls
Official ID Z-2069-2026 · Official record ↗
If the connection between a mint Lesion workstation and the mint Lesion server is interrupted while performing a read, in rare cases some information may be lost or incorrectly lin…
Company / brand: Mint Medical recalls
Official ID Z-2068-2026 · Official record ↗
Contamination to in-vitro diagnostic test may result in false positives.
Company / brand: BioFire Diagnostics recalls
Official ID Z-2067-2026 · Official record ↗
Some defibrillators serviced between July 2023 through November 2025 were serviced without objective evidence that a Performance Inspection Procedure (PIP) was conducted, and the i…
Company / brand: Physio-Control recalls
Official ID Z-2065-2026 · Official record ↗
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water fl…
Company / brand: Erbe Medical recalls
Official ID Z-2064-2026 · Official record ↗
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water fl…
Company / brand: Erbe Medical recalls
Official ID Z-2063-2026 · Official record ↗
Devices providing sterile water/CO2/air to endoscopes were manufactured with a distal irrigation segment connector configuration that may be more susceptible to unintended water fl…
Company / brand: Erbe Medical recalls
Official ID Z-2062-2026 · Official record ↗
Due to a manufacturing issue (i.e. malfunctioning of electrical Leakage tester).
Company / brand: Spacelabs Healthcare recalls
Official ID Z-2052-2026 · Official record ↗
Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.
Company / brand: Centinel Spine recalls
Official ID Z-2051-2026 · Official record ↗
Product labeling mix up. The prodisc C SK U.S. Implant Extra Large 6mm product was labeled as a 5mm and prodisc C SK U.S. Implant Extra Large 5mm product was labeled as a 6mm.
Company / brand: Centinel Spine recalls
Official ID Z-2050-2026 · Official record ↗
For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for Bradyarrhy…
Company / brand: Boston Scientific recalls
Official ID Z-2049-2026 · Official record ↗
For some patients upgraded from a LUX-Dx M301 device to a new Model M302 or M312, the new ICM device is not collecting PVC Burden data (both M302/M312) or monitoring for Bradyarrhy…
Company / brand: Boston Scientific recalls
Official ID Z-2048-2026 · Official record ↗
Due to manipulator containing screws with in the arm sub-assembly that my be susceptible to breaking.
Company / brand: Intuitive Surgical recalls
Official ID Z-2046-2026 · Official record ↗
Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold"
Company / brand: Medical Action Industries recalls
Official ID Z-2007-2026 · Official record ↗
Impacted kits contain syringes recalled by Medline Industries. Syringe rotating adaptor may unwind during use, which may result in a loose connection or full disconnection between …
Company / brand: American Contract Systems recalls
Official ID Z-1981-2026 · Official record ↗
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Company / brand: AVID Medical recalls
Official ID Z-1979-2026 · Official record ↗
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Company / brand: AVID Medical recalls
Official ID Z-1978-2026 · Official record ↗
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Company / brand: AVID Medical recalls
Official ID Z-1977-2026 · Official record ↗
Potential risk for Medline syringe rotating adaptor unwinding during use, which may result in a loose connection and/or full disconnection between the syringe and manifold.
Company / brand: AVID Medical recalls
Official ID Z-1976-2026 · Official record ↗
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Government sources last checked October 22, 2026 at 12:00 PM UTC.