These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.

High Risk Recalls

3,609 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.

What to do if you own a recalled product:

  1. Stop using the product immediately
  2. Keep the product away from children
  3. Follow the remedy instructions provided
  4. Contact the manufacturer for a refund or replacement
Recalled Happiness Light LED Lights
HIGH
CPSC

Happiness Light LED Lights Recalled for Battery Ingestion Risk (2026)

Happiness Light recalled LED lights sold on Amazon after determining two CR2032 lithium coin batteries inside the unit could be accessed by children. Each light contains two coin batteries. Consumers should stop using the recalled lights and request a full refund by emailing usa@happinesslight.com.

LED Lights
The recalled
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Recalled SCUBAPRO Monorail Weight Pockets Shown in all colors and sizes
HIGH
CPSC

SCUBAPRO Recalls Monorail Weight Pockets for BCDs Over Entrapment Risk (2026)

SCUBAPRO recalled Monorail Weight Pockets for BCDs sold by retailers worldwide on 2026-04-09 after safety reviews identified a serious entrapment risk. The recall notes a potential for entrapment and drowning and cites missing warning labels. Consumers should stop using the recalled bed rails and contact SCUBAPRO for a full refund.

SCUBAPRO
The D-ring
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Recalled BISSELL Steam Shot OmniReach Steam Cleaner with Attachments
HIGH
CPSC

BISSELL Recalls 1 Million Steam Shot OmniReach Cleaners Over Burn Hazard (2026)

BISSELL recalled more than 1 million Steam Shot OmniReach handheld steam cleaners with attachments, sold nationwide through retailers. The attachments can detach and expel hot water or steam, posing a serious burn hazard. Stop using the attachments immediately and contact BISSELL to receive free replacement attachments.

BISSELL
The recalled
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Recalled Wybot S1 (Top)
HIGH
CPSC

Wybotics Recalls Osprey 700 Max and S1 Robotic Pool Vacuums for Burn and Fire Hazards (2026)

Wybotics is recalling specific Osprey 700 Max and S1 robotic pool vacuums sold through retailers after reports that the lithium-ion battery can overheat, creating a burn and fire hazard. The recall covers Osprey 700 Max models WY3312MAX and WY100MAX and S1 WY200, with serial numbers WY100M230117XXXX, WY100M230127XXXX, WY100M230130XXXX, WY100M230318XXXX, WY200-230328XXXX and W200**230330XXXX. The U

Wybotics, Co. Ltd. of Tianjin, Chin
The lithium-ion
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Recalled Prestige Lighter – Supernova, gray
HIGH
CPSC

Prestige Import Group Recalls 2 Prestige Supernova and Typhoon Lighters for Fire Hazard (2026)

Prestige Import Group recalled two Prestige-branded metal butane torch lighters sold by small independent stores nationwide and online at prestigeimportgroup.com from October 2023 through March 2026 for $7 to $10. The lighters lack a required child-resistant mechanism and failed pre-market submissions, creating a risk of serious burn injuries or fires. Consumers should stop using the recalled ligh

Prestige Import Group
The recalled
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Recalled Shenzhen Shijingjie Network Technology Extension Cord – blue
HIGH
CPSC

Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled in 2026 Walmart Recall

Shenzhen Shijingjie Network Technology recalled two models of male-to-male extension cords sold at Walmart after safety concerns. The cords pose a risk of electrocution and carbon monoxide poisoning when used for backfeeding from a generator into a home. Consumers should stop using the recalled cords immediately and contact the company for a full refund.

Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords
The recalled
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HIGH
FDA DEVICE

Medtronic SynchroMed Flex Infusion Mode - A810 Clinician Programmer Software Application, loaded on the following devices: 1. PROG CT900A CLINICIAN TABLET US, Model Number CT900A; 2. PROG...

Software issue: When programming the SynchroMed Pump with the A810 CP App in Flex Infusion Mode, the infusion steps should automatically be arranged in consecutive order, from earliest to latest. However, in rare cases, the steps may be displayed out of order. If this occurs, the programmed Flex Infusion schedule will not be delivered at the intended time, if at all.

Medtronic Neuromodulation
Software issue:
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HIGH
FDA DEVICE

Swan-Ganz Pacing Catheter, Models: D200F7;

Catheters may, due to a manufacturing process and material changes, leak/break from the (blue) proximal injectate lumen hub, which may lead to infection, medication loss, and/or blood loss.

Becton, Dickinson and
Catheters may,
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Vehicles & Parts
HIGH
NHTSA

BMW Recalls 3 EV Models IX, I7 and i4 Over High-Voltage Battery Issue (2026)

BMW recalls 2022-2025 IX, 2023-2024 I7, and 2022-2023 i4 electric vehicles sold at BMW dealerships. A high-voltage battery cell module may have been improperly assembled. This can stress the module frame and lead to module failure. Owners should contact BMW for a free replacement of affected modules; recall letters were mailed September 11, 2025.

BMW
Battery module
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