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.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate drums, Model Number 13-2251-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate drums, Model Number 13-2201-5 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate drums, Model Number 13-1251-1 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-4231-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-3301-2 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-3251-9 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-3231-1 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-3201-4 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-2351-8 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-2301-3 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-2251-0 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-2231-2 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-2201-5 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-1301-4 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-20FDA-DeviceFresenius Medical Care Holdings, Inc.Class IINaturaLyte Liquid Acid concentrate bottles, Model Number 08-1251-1 - Product Usage: used in conjunction with Fresenius Renal Technologies Sodium Bicarbonate Concentrate in a compatible 45X dilution three-stream artificial kidney (hemodialysis) machine.
The sodium and/or calcium levels in these concentrates were below the manufacturing specifications.
- 2021-01-15USDAPublic Health AlertFSIS Issues Public Health Alert for Beef Jerky Products Due to Misbranding and an Undeclared Allergen
Misbranding, Unreported Allergens
- 2021-01-14CPSCScalpa Inc., of Phoenix, Ariz.Scalpa Recalls Scalpa Numb Maximum Strength Topical Anesthetic Cream Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)
The product contains the substance lidocaine 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 to young children.
- 2021-01-13CPSCJuratoys US Corp., Millersburg, Pa.Juratoys Recalls Toy Trumpets Due to Choking Hazard
The small plastic pieces inside the toy trumpets can come loose and can be ingested by children, posing a choking hazard.
- 2021-01-07CPSCNoble House Home Furnishings LLC, of Chatsworth, Calif.Noble House Home Furnishings Recalls Chests, Cabinets and Dressers Due to Tip-Over and Entrapment Hazards (Recall Alert)
The recalled chests, cabinets and dressers 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).
- 2020-12-31USDAPublic Health AlertFSIS Issues Public Health Alert for Frozen, Fully Cooked, Not Shelf Stable Chicken Sriracha Ravioli Products Due to Misbranding and an Undeclared Allergen
Misbranding, Unreported Allergens
- 2020-12-30CPSCTarget Corp., of Minneapolis, Minn.Target Recalls Infant-Toddler Girl's One-Piece Rashguard Swimsuits Due to Choking Hazard
The snaps can break or detach from the suits, posing choking and laceration hazards to children.
- 2020-12-30CPSCTarget Corp., of Minneapolis, Minn.Target Recalls Infant Rompers Due to Choking Hazard
The snaps can break or detach from the rompers, posing a choking, laceration and pinching hazards to children.
- 2020-12-23FDA-DeviceCarl Zeiss Meditec AGClass IICarl Zeiss Meditec AG VISUREF150 REF 2227-967 - Product Usage: is a diagnostic instrument used to determine the objective refractive values and keratometric characteristics of the human eye. The results are used to assist the process of prescribing optical aids such as eyeglasses and contact lenses.
Due to the incorrect DC/DC converter being assembled onto the communication board. As a result the effectiveness of the communication board cannot be guaranteed in that the safety function of the board would be insufficient resulting in an increased leakage of current and potentially cause electrical shocks to the user.
- 2020-12-23FDA-DrugSimex Logistics SA de CVClass IICitruGel Hand Sanitizer Advanced Formula 70% Alcohol Fresh Lemon Scent, 33.81 FL OZ (1L), Distributed By Citru Gel Inc. Henderson, NV 89052 www.citrugel.com NDC: 78247-002-01
Subpotent drug
- 2020-12-23CPSCGSK Consumer Healthcare, of Warren, N.J.GSK Consumer Health Recalls Five Excedrin Brands Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
Some of the bottles containing the over-the-counter drug can have a hole in the bottom. If there is a hole, children could access and swallow the contents, posing a risk of poisoning. These products contain the substances aspirin and acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA).
- 2020-12-17CPSCOtis Elevator Company of Farmington, Ct.Otis Elevator Company Recalls to Inspect Private Residence Elevators Due to Entrapment Hazard; Risk of Serious Injury or Death to Young Children
Children can become entrapped in the space between the exterior landing (hoistway) door and the interior elevator car door or gate, and suffer serious injuries or death when the elevator is called to another floor.
- 2020-12-16FDA-FoodVeg Pro International IncClass I1. Fresh Attitude Baby Spinach, 11 oz. 2. Fresh Attitude Baby Spinach, 5 oz.
Spinach may be contaminated with Salmonella
- 2020-12-16CPSCGraco Children's Products Inc., of Atlanta, Ga.Graco Recalls Inclined Sleeper Accessory Included with Four Models of Playards to Prevent Risk of Suffocation
Infant fatalities have been reported with other manufacturers' inclined sleep products, after infants rolled from their back to their stomach or side while unrestrained, or under other circumstances.
- 2020-12-10CPSCShenzhen Luosi Ge Trading Co., of China (owner of Homfa trademark)Homfa Cabinets Recalled Due to Tip-Over and Entrapment Hazards; Made by Shenzhen Luosi Ge Trading Co. (Recall Alert)
The recalled cabinets are unstable if not anchored to the wall, posing tip-over and entrapment hazards that can result in death or serious injuries to children. The cabinets do not comply with the performance requirements of the U.S. voluntary industry standard (ASTM F2057-19).
- 2020-12-09CPSCWashington Shoe Company, of Kent, Wash.Washington Shoe Company Recalls Western Chief Toddler Boots Due to Choking Hazard; Sold Exclusively at Target
Rivets used to attach the handles to the boot can detach, posing a choking hazard to children.
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