Baby and kids' product recalls

6672 federal recalls on file. Every federal recall touching baby and kids' products — toys, formula, baby food, cribs, strollers, child seats. Sourced from CPSC, FDA, USDA, and NHTSA, translated into plain English.

2020-07-02CPSCNorth Woods General Store LLS, d/b/a A Better You!, of Hebron, Ky.
A Better You! Recalls Belecoo Strollers Due to Violation of Federal Stroller and Carriage Safety Standard; Fall, Entrapment and Strangulation Hazards (Recall Alert)
The recalled strollers violate the federal Carriages and Strollers standard. A child's torso can pass through the opening between the activity tray and the seat bottom and his/her head can become entrapped, posing entrapment and strangulation hazards. The location of the crotch restraint creates a large opening between the seat bottom and the restraint, and it can become detached, posing a fall hazard to children.
2020-07-02CPSCAvalon Furniture, of Houston, Texas
Avalon Furniture Recalls Cottage Town Bedroom Furniture Sold at Rooms To Go Due to Violation of Federal Lead Paint Ban; Risk of Poisoning (Recall Alert)
The base coat paint used on pieces within the furniture collection contains levels of lead that exceed the federal lead paint standard. Lead is toxic if ingested by young children and can cause adverse health effects.
2020-07-01FDA-DeviceArgon Medical Devices, IncClass II
BioPince Full Core Biopsy Instrument 16ga x 15cm.,Use with Optional CO-Axial Needle MCXS1615BP. QTY.: 5/CS - Product Usage: The disposable, automatic BioPince Full Core Biopsy Instrument is used to obtain multiple core samples from soft tissue such as liver, kidney, abdominal masses, etc.
Incorrect product labeling.
2020-07-01FDA-DrugAlembic Pharmaceuticals LimitedClass II
Aripiprazole Tablets, USP, 2 mg, 30 Tablets per bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation Division) Panelav 389350, Gujarat, India Manufactured for: Alembic Pharmaceuticals, Inc. 750 Route 202, Bridgewater, NJ 08807 USA, NDC 62332-097-30.
Labeling: Label mix up: Bottles labeled as aripiprazole 2 mg, 30 count had aripiprazole 5 mg tablets, 100 count.
2020-07-01CPSCSymbol Arts LLC, of Ogden, Utah
Boy Scouts of America Recalls Cub Scout Activity Pins Due to Violation of the Federal Lead Content Ban
The pin's face and shaft contain levels of lead that exceed the federal lead content ban. Lead is toxic if ingested by young children and can cause adverse health issues.
2020-06-25CPSCGoPlus Corp. d/b/a Costway Inc., of Fontana, Calif.
Costway Recalls Baby Strollers Due to Violation of Federal Stroller and Carriage Safety Standard; Fall, Entrapment and Strangulation Hazards (Recall Alert)
The recalled strollers violate the Federal Standard for Carriages and Strollers. A child's torso can pass through the opening between the activity tray and the seat bottom and his/her head can become entrapped, posing entrapment and strangulation hazards. The location of the crotch restraint creates a large opening between the seat bottom and the restraint, posing a fall hazard to children.
2020-06-24FDA-DeviceGE Healthcare, LLCClass II
Giraffe Incubator with installed Servo Oxygen module. Infant incubator.
Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a different environmental oxygen level than what is displayed by the device, if a certain optional component referred to as the Servo Oxygen Module is installed.
2020-06-24FDA-DeviceGE Healthcare, LLCClass II
Giraffe OmniBed with installed Servo Oxygen module. Infant incubator and warmer.
Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a different environmental oxygen level than what is displayed by the device, if a certain optional component referred to as the Servo Oxygen Module is installed.
2020-06-24FDA-DrugEco Lips IncClass II
EcoLips Sport Lip Balm, SPF 30, Avobenzone (5%), Octinoxate (10%), Octisalate (5%), Net Wt. 0.15 oz. (4.25g) tube, Eco Lips, Inc., Marion, IA 52302, UPC: 859623000030; 859623000177; 859623000573; Display UPC: 859623000092; 859623000108; 859623000139; 859623000146; 859623000184; 859623000535; 859623001037.
Superpotent Drug: The active ingredient, avobenzone, is used at 5% which is higher than the allowable 3% in the sunscreen formula per FDA sunscreen regulations.
2020-06-18CPSCModus Furniture, of Los Angeles, Calif.
Modus Furniture Recalls Dressers Due to Tip-Over and Entrapment Hazards: In-Home Remedy May be Delayed Due to COVID-19 Restrictions; Keep Product Away from Children (Recall Alert)
The recalled dressers are unstable if the mirror is not installed, posing serious tip-over and entrapment hazards that can result in death or injuries to children. The dressers do not comply with one of the performance requirements of the U.S. voluntary industry standard (ASTM 2057-17). The tip-over restraint kits do not comply with the performance requirements of the U.S. voluntary industry standard (F3096-14).
2020-06-17FDA-DevicePhysio-Control, Inc.Class II
Infant Child Starter Kits, Part Number: 3202784-009, containing Infant/Child Reduced Energy Defibrillation Electrodes, for use with LIFEPAK 1000 defibrillator, LIFEPAK 500 defibrillator, and LIFEPAK CR Plus/EXPRESS defibrillator - Product Usage: intended to be used by personnel who are trained on the device operation and in basic life support or other physician-authorized emergency medical response system.
Packaging of infant child reduced energy electrodes was not properly sealed.
2020-06-17FDA-DevicePhysio-Control, Inc.Class II
Infant/Child Reduced Energy Defibrillation Electrodes, Part Number: 3202380-006, for use with LIFEPAK 1000 defibrillator, LIFEPAK 500 defibrillator, and LIFEPAK CR Plus/EXPRESS defibrillator - Product Usage: intended to be used by personnel who are trained on the device operation and in basic life support or other physician-authorized emergency medical response system.
Packaging of infant child reduced energy electrodes was not properly sealed.
2020-06-11CPSCDavina Wellness, of Mapleton, Utah
Davina Wellness Recalls Wintergreen Essential Oil and Essential Oil Blend with Wintergreen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The products contain the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
2020-06-11CPSCBonnsu LLC, of Sausalito, Calif. doing business as Miniware
Bonnsu Recalls Miniware Teething Spoons Due to Choking Hazard
The teething spoon can break in a child's mouth when being used as a teether, posing a choking hazard to infants.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATION 10 CC IMPACT FORMULA. REF/UDI: 390-2110/ /00813845021092 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATION 5CC IMPACTFORMULA. REF/UDI: 390-2105/00813845020085 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATION 3CC IMPACTFORMULA. REF/UDI: 390-2103/00813845020078 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATIONEX 3CC IMPACTFORMULA. REF/UDI: 390-0203/00813845020030 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATIONEX 5CC IMPACTFORMULA. REF/UDI: 390-0205/00813845020047 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATION 10CC INJECT FORMULA. REF/UDI: 390-2010/00813845020061 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATION 5CC INJECT FORMULA. REF/UDI: 390-2005/00813845020054 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATIONEX 5CC INJECT FORMULA. REF/UDI: 390-0005/00813845020023 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATIONEX 3CC INJECT FORMULA. REF/UDI: 390-0003/00813845020016 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10FDA-DeviceOsteomed, LLCClass II
OSTEOVATIONEX 2CC INJECT FORMULA. REF/UDI: 390-0002/00813845020009 - Product Usage: The product provides a bone void filler that is replaced by bone during the healing process.
Incorrect shelf-life for bone void filler kits; the product may not maintain its setting characteristics for the labeled shelf-life duration.
2020-06-10CPSCIsland Wear. Inc., of Ocean City, Md.
Island Wear Recalls Strollers Due to Violation of Federal Stroller and Carriage Safety Standard; Fall and Choking Hazards
The recalled strollers violate the federal Carriages and Strollers Safety standard. The location of the restraint system creates a large gap between the restraint and the seat. The child can slip through the gap, posing a fall hazard. In addition, the covering on the grab bar can detach and expose foam, posing a choking hazard to children.
2020-06-04CPSCTim Trading LLC, of Rowland Heights, Calif.
Tim Trading Recalls Emori Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
2020-06-04CPSCCapstone Holdings LLC, dba Simply Earth, of Waldo, Wis.
Capstone Holdings Recalls Simply Earth Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
2020-05-27CPSCSanvall Enterprises Inc., of Doral, Fla.
Sanvall Enterprises Recalls Rapid Alivio Pain Relieving Roll-On Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
2020-05-21CPSCHerman Miller Inc., of Zeeland, Mich.
Herman Miller and Design Within Reach Recall Dressers and Cabinets Due to Tip-Over and Entrapment Hazards; Remedy May Be Delayed Due to COVID-19 Restrictions; Keep Product Away from Children (Recall Alert)
The recalled dressers and cabinets are unstable and can tip over if not anchored to the wall, posing serious tip-over and entrapment hazards that can result in death or injuries to children. The chests do not comply with the performance requirements of the U.S. voluntary industry standard (ASTM F2057-19).
2020-05-21CPSCViva Doria, Inc. of Redmond, Wash.
Viva Doria Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The product contains the substance methyl salicylate which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the product is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.

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