Recalls published in April 2026
Everything the FDA, USDA FSIS, CPSC and NHTSA announced in April 2026, newest first.
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Highest risk · 6 months ago
Thermos 8.2 Million Stainless King Food Jars and Bottles recall: Serious Impact Injury and Laceration Hazards
Serious Impact Injury and Laceration Hazards
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Highest risk · 6 months ago
Segmart 4-Drawer Dressers recall: The recalled dressers are unstable if they are not anchored to the wall
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious…
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Highest risk · 6 months ago
Residential Elevators Elevator StrikeLock Hoistway Door Locking Device recall: Risk of Serious Injury or Death from Fall and Injury Hazards
Risk of Serious Injury or Death from Fall and Injury Hazards
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Highest risk · 6 months ago
Qumeney Bicycle Light Sets recall: The recalled bicycle lights violate the mandatory standard for consumer
The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell…
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Highest risk · 6 months ago
Dgivovo US Electric Pressure Washers recall: The recalled pressure washers lack an integral ground-fault
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI), posing a serious risk of injury or death from shock and…
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Highest risk · 6 months ago
Malker Bicycle Light Sets recall: The recalled bicycle lights violate the mandatory standard for consumer
The recalled bicycle lights violate the mandatory standard for consumer products with button cell and coin batteries because they contain button cell…
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Highest risk · 6 months ago
Tonyidea Earthtec 7 3/8 Inch Pool Drain Covers recall: The recalled drain covers violate the entrapment protection standards
The recalled drain covers violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act (VGBA), posing entrapment…
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Highest risk · 6 months ago
CBC Group Stephan Baby Boo Bunnie and Friends Children's Toys recall: Risk of Serious Injury from Choking and Laceration Hazards
Risk of Serious Injury from Choking and Laceration Hazards
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Highest risk · 6 months ago
Build-A-Bear Workshop Heartwarming Hugs Bears recall: Risk of Serious Injury or Death from Choking Hazard to Children
Risk of Serious Injury or Death from Choking Hazard to Children
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Highest risk · 6 months ago
Bayer 6 mL Size Afrin Original Nasal Spray Bottles recall: Risk of Serious Injury or Illness from Child Poisoning
Risk of Serious Injury or Illness from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging
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Highest risk · 6 months ago
American Honda Motor Off-Road Motorcycles recall: Risk of Serious Injury or Death Due to Crash Hazard
Risk of Serious Injury or Death Due to Crash Hazard
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Highest risk · 6 months ago
Alliance Chemical 1-K Kerosene Heater Fluid Containers recall: Risk of Serious Injury or Death from Flash Fire
Risk of Serious Injury or Death from Flash Fire, Burn and Child Poisoning; Violates Mandatory Standards for Portable Fuel Containers
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Highest risk · 6 months ago
Mobility Source Medical Technology Co., Ltd. of China Hepo Adult Portable Bed Rails recall: The recalled bed rails violate the mandatory standard for adult portable bed
The recalled bed rails violate the mandatory standard for adult portable bed rails because users can become entrapped within the bed rail or between…
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Elevated risk · 6 months ago
Acer America Corporation Two-Wheeled Folding Electric recall: Risk of Injury from Fall Hazard
Risk of Injury from Fall Hazard
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Highest risk · 6 months ago
Uhomepro 5-Drawer Dressers recall: The recalled dressers are unstable if they are not anchored to the wall
The recalled dressers are unstable if they are not anchored to the wall, posing tip-over and entrapment hazards that can result in risks of serious…
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Public Health Alert · 6 months ago
FSIS Issues Public Health Alert for Various Meat and Poultry Products Containing FDA-Regulated Dairy Products That Have Been Recalled Due to Possible…
Product Contamination
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Class II · 6 months ago
Olympus Corporation of the Americas OER-ELITE Endoscope Reprocessor Connecting Tubes recall: Potential for the Version 2 reprocessor connecting tube lock levers may fail
Potential for the Version 2 reprocessor connecting tube lock levers may fail prematurely.
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Class II · 6 months ago
Medline Convenience Kits containing select SKUs of 10mL Polycarbonate recall: Unapproved design changes to the products outside of the 510(k) clearance
Unapproved design changes to the products outside of the 510(k) clearance.
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Class II · 6 months ago
Medline Kits: 1) Arthrogram Tray recall: The 510(k) regulatory clearances for certain Control Syringes
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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Class II · 6 months ago
Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator recall: The catheter inflation tag attached to the device may contain an incorrect
The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures…
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Class II · 6 months ago
Medline Kits: 1) D AND C PACK recall: The 510(k) regulatory clearances for certain Control Syringes
The 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded.
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Class II · 6 months ago
Angiodynamics, Inc. Soft-Vu Angiographic Catheter, Headhunter , Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…
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Class II · 6 months ago
XTANT Medical Holdings, Inc nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus recall: Products were incorrectly labeled with a 5-year shelf life. The approved
Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
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Class II · 6 months ago
Angiodynamics, Inc. Soft -Vu Angiographic Catheter, Kumpe, Non-Braided recall: The affected devices contain a manufacturing defect which may prevent
The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID)…