United States Recalls

Consumer recalls from the FDA, CPSC, NHTSA, and USDA FSIS.

Showing 24 of 16,409 results
Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury...
CPSCGeneral Alert

Yamazuki Recalls Youth All-Terrain Vehicles (ATVs) Due to Risk of Serious Injury...

The recalled youth ATVs violate the mandatory safety standard for ATVs because they are missing brake lights, reducing visibility of the youth ATV to other vehicles, posing a deadly crash hazard.

Jun 25, 2026Yongkang Ruihe Metal Products Co. Ltd., of China
Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from ...
CPSCGeneral Alert

Montessori Busy Board Toys Recalled Due to Risk of Serious Injury or Death from ...

The busy boards violate the mandatory safety standard for toys because magnets can detach, posing a deadly ingestion hazard. When high-powered magnets are swallowed, the ingested magnets can attract each other, or other metal objects and become lodged in the digestive system. This can result in perforations, twisting, and/or blockage of the intestines, blood poisoning and death.

Jun 25, 2026
Safety Alert
RSS FeedGeneral Alert

Revival Animal Health, LLC Voluntarily Recalls Canine and GM Milk Replacers Due to Low or Elevated Levels of Vitamin D

Jun 25, 2026
Food & Beverage
USDA FSISClass I

Reser’s Fine Foods, Inc. Recalls Ready-To-Eat Pasta Salad Product Due to Misbran...

Misbranding, Unreported Allergens

Jun 25, 2026Reser's Fine Foods
Safety Alert
RSS FeedGeneral Alert

Lehi Valley Trading Company Issues Allergy Alert on Undeclared Peanuts in Chocolate Covered Raisins

Jun 25, 2026
Super Off-Road Solar Power Banks Recalled Due to Overheating; Imported by Specto...
CPSCGeneral Alert

Super Off-Road Solar Power Banks Recalled Due to Overheating; Imported by Specto...

The solar power bank's lithium-ion battery can swell and overheat, posing a burn hazard to consumers.

Jun 25, 2026
Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Hea...
CPSCGeneral Alert

Daikin Comfort Technologies Manufacturing Recalls Amana Air Conditioners and Hea...

The heating element can remain energized during a ground fault, despite being turned off, posing a risk of fire or burn injury to consumers.

Jun 25, 2026
Kith Retail Recalls Children's Loungewear Sets Due to Risk of Serious Injury fro...
CPSCGeneral Alert

Kith Retail Recalls Children's Loungewear Sets Due to Risk of Serious Injury fro...

The recalled children's loungewear sets violate the mandatory flammability standards for children's sleepwear, posing a risk of serious burn injuries.

Jun 25, 2026
Shield Line Recalls MedPride Baby Oil Bottles Due to Risk of Serious Injury or D...
CPSCGeneral Alert

Shield Line Recalls MedPride Baby Oil Bottles Due to Risk of Serious Injury or D...

The baby oil contains low-viscosity hydrocarbons, which must be in child-resistant packaging, as required by the Poison Prevention Packaging Act. The baby oil's packaging is not child-resistant, posing a risk of serious injury or illness from poisoning if the contents are swallowed by young children. Additionally, petroleum distillates can get into the lungs, causing chemical pneumonia and/or pulmonary damage, which can be fatal.

Jun 25, 2026
Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injur...
CPSCGeneral Alert

Southern Telecom Expands Recall of Lomi Waxing Kits Due to Risk of Serious Injur...

The roll-on warmers' power cord can overheat and short circuit, posing a risk of serious injury or death from fire, burn and electrical shock hazards.

Jun 25, 2026
Honlyne LED Party Favors Recalled Due to Risk of Serious Injury Death from Batte...
CPSCGeneral Alert

Honlyne LED Party Favors Recalled Due to Risk of Serious Injury Death from Batte...

The LED party favors violate the mandatory safety standard for consumer products because the battery compartment within the light-up products contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.

Jun 25, 2026
Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death...
CPSCGeneral Alert

Raychy Children's Light Sneakers Recalled Due to Risk of Serious Injury or Death...

The recalled sneakers violate the mandatory standard for consumer products with button cell and coin batteries because the lithium coin batteries can be accessed easily by children, posing an ingestion hazard.?Additionally, the packaging and product do not have the warnings required under?Reese's Law. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns, and death.

Jun 25, 2026
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: 1) BR L&D PACK, Medline Kit Number...

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass II

HarmonyAIR A-Series Surgical Lighting System

The the plus and minus buttons (+/-) used to control light intensity on the light heads may detach.

Jun 24, 2026Steris Corporation
Pharmaceutical
FDA DrugsClass II

Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Medical Device
FDA DevicesClass I

Description/REF: CVC/PSI KIT: 2 LUMEN 8 FR X 6 IN/ASK-42802-PLH; CVC KIT: 3-LUME...

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass II

MEDLINE Medical Procedure Kits labeled as: 1) KIT UROLOGY URETHROPLASTY, Medl...

During an internal review, Medline identified representative samples did not meet applicable performance specifications. Identified issues include irregularities in catheter surface finish, instances where the catheter connector detached prematurely from the catheter funnel, and limited cases where the catheter outer diameter did not meet specification.

Jun 24, 2026Medline Industries, LP
Medical Device
FDA DevicesClass I

Description/REF: MIDLINE CATHETER KIT: 3 FR X 20 CM/CDC-02031-MK1A; AM/AT PI MID...

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass I

Description/REF: PERITONEAL LAVAGE CATH KIT:8FR/AK-09000

Lidocaine, Bupivacaine, and 0.9% sodium chloride, the subject of a supplier recall, were included into kits and sets. The supplier was found to have quality issues and limited reports of drug ineffectiveness, and if sterility of a water-based injectable product is compromised this could lead to serious or life-threatening injuries.

Jun 24, 2026ARROW INTERNATIONAL, LLC
Medical Device
FDA DevicesClass II

Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Pr...

Due to a software coding issues for calculating the implant orientation diagram printout for the implantation for toric implantable collamer lenses.

Jun 24, 2026Staar Surgical AG
Pharmaceutical
FDA DrugsClass II

Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomyc...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Medical Device
FDA DevicesClass II

Medline CCI Nerve Block Tray DYNJRA2742 Medline CPNB DYNJRA2716

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP
Pharmaceutical
FDA DrugsClass II

Med Pride, Triple Antibiotic Ointment, Bacitracin Zinc 400 units, Neomycin Sulfa...

CGMP Deviations; deficiencies observed during FDA inspection

Jun 24, 2026Dabur India Limited
Medical Device
FDA DevicesClass II

Medline convenience kits: DRIVELINE MANAGEMENT KIT EBSI1688 PORT DRESSING...

Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.

Jun 24, 2026Medline Industries, LP