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

456 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 IcyBreeze Buddy Portable Misting Fan in slate blue
HIGH
CPSC

IcyBreeze Recalls Misting Fans Over Fire Hazard Risk

IcyBreeze recalled its Buddy portable misting fan on September 18, 2025, due to a fire hazard. The device can overheat while charging, posing a risk of ignition. Consumers should stop using the fan immediately and return it for a full refund.

IcyBreeze Cooling
The misting
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Recalled Five Below Tabletop Fire Pit – smooth model
HIGH
CPSC

Five Below Recalls Tabletop Fire Pits Over Burn Hazard

Five Below recalled two models of tabletop fire pits due to burn hazards. The recall affects products sold from April 2024 through August 2025. Consumers reported risks of flash fires and flame jetting causing serious injuries.

Five Below
Alcohol fuel
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Recalled Youbeien Crib Mobile in pink
HIGH
CPSC

Youbeien Crib Mobiles Recalled Over Battery Ingestion Risk

Youbeien recalled crib mobiles on September 18, 2025, due to a risk of battery ingestion. The toys fail to meet safety standards and pose serious injury risks. Consumers should stop using the mobiles and contact GKKBSJ for refunds.

Youbeien
The recalled
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Recalled YooxArmor Multi-Purpose Helmet (front view)
HIGH
CPSC

YooxArmor Recalls Kids' Helmets for Serious Injury Risk

YooxArmor recalled multi-purpose kids' helmets on September 18, 2025. The helmets violate safety standards and pose a risk of serious head injuries. Consumers should stop using the helmets immediately and contact YooxArmor for a refund.

YooxArmor
The recalled
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Recalled EnHomee 13-drawer dresser (front)
HIGH
CPSC

EnHomee Dressers Recalled Due to Tip-Over Hazard

EnHomee recalled its Fabric 13-Drawer Dressers on September 18, 2025. The dressers pose a serious tip-over risk if not anchored to a wall. This recall affects an unspecified number of units sold by EnHomee Direct.

EnHomee Dressers
The recalled
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HIGHFDA DRUG

Glenmark Pharmaceuticals Recalls Azelaic Acid Gel Over Texture Issues

Glenmark Pharmaceuticals Inc. recalled 13,824 tubes of Azelaic Acid Gel on September 17, 2025. The recall stems from market complaints regarding a gritty texture. Consumers should stop using the product immediately and contact their healthcare provider.

Glenmark Pharmaceuticals
CGMP Deviations:
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HIGHFDA DRUG

Skin MD Body Acne Cleanser Recalled Due to Benzene Contamination

Skin MD by Dr Monika Kiripolsky recalled its Body Acne Cleanser on September 12, 2025. The recall follows the discovery of elevated benzene levels in the product. This contamination poses a high health risk to consumers in California and Georgia.

Skin MD
Chemical Contamination:
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Recalled In My Jammers Button Up Flare Set – Victoria print
HIGH
CPSC

In My Jammers Recalls Pajama Sets Over Burn Hazard

In My Jammers recalled children's button flare pajama sets due to a burn hazard on September 11, 2025. The pajamas violate mandatory flammability standards, posing a risk of injury to children. Consumers should stop using the pajamas immediately and return them for a full refund.

In My Jammers
The recalled
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Recalled Shierdu Wooden Cactus Toy -packaging
HIGH
CPSC

Shierdu Children's Toys Recalled Over Choking Hazard Risk

Shierdu recalled children's wooden building block cactus toys on September 11, 2025. The toys pose a choking hazard, violating the small parts ban. Consumers should stop using them immediately and seek a refund.

Shierdu Children's Toys
The recalled
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HIGHFDA DEVICE

Biomet Recalls Juggerknot Mini Soft Anchors Due to Labeling Error

Biomet recalled 40 units of Juggerknot Mini Soft Anchors on September 9, 2025. The recall stems from a labeling error where the carton contains 1.4mm Short devices instead of the labeled 1.0mm Mini products. Patients and healthcare providers must stop using these devices immediately.

Biomet
The outer
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