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.
- 2018-05-16FDA-DeviceVyaire MedicalClass IAirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, PEEP valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.
- 2018-05-16FDA-DeviceVyaire MedicalClass IAirLife Resuscitation, Infant, with mask, oxygen reservoir bag, pressure-relief valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.
- 2018-05-16FDA-DeviceVyaire MedicalClass IAirLife Resuscitation, Infant, with mask, 28inch large bore tubing, pressure-relief valve Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.
- 2018-05-16FDA-DeviceVyaire MedicalClass IAirLife Resuscitation, Infant, with mask, 40 inch oxygen reservoir tubing, pressure-relief valve, CO2 detector, manometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.
- 2018-05-16FDA-DeviceVyaire MedicalClass IAirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, Broselow Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.
- 2018-05-16FDA-DeviceVyaire MedicalClass IAirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, CO2 monitor, monometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.
- 2018-05-16FDA-DeviceVyaire MedicalClass IAirLife Resuscitation, Infant, with mask, 40inch oxygen reservoir tubing, pressure-relief valve, manometer Product Usage: The AirLife Resuscitation devices are manual resuscitation devices that are used to provide positive pressure ventilation to patients who are not breathing or cannot adequately breathe on their own.
The mask component on various lots of the resuscitation devices have been identified as having the potential to exhibit a sticking condition which may result in a difficult to/unable to disconnect condition of the mask from the elbow of the resuscitator.
- 2018-05-16FDA-FoodTRIANGLE PHARMANATURALS LLCClass IChameleon Kratom Formula 51 in 60 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
- 2018-05-16FDA-FoodTRIANGLE PHARMANATURALS LLCClass IChameleon Kratom Formula 27 in 60 capsule plastic bottles; Manufactured for Raw Form Organics, Las Vegas, NV 89118 by Triangle Pharmanaturals, LLC, Las Vegas, NV 89119
All Kratom products manufactured, processed, packed, and/or held by Triangle Pharmanaaturals LLC have the potential to be contaminated with Salmonella
- 2018-05-16CPSCPlay and Park Structures, Fort Payne, Ala.Play and Park Structures Recalls Playground Slides Due to Entrapment Hazard (Recall Alert)
A gap between the rails near the entrance way to the slide poses an entrapment hazard to young children.
- 2018-05-16USDAClass IICheck Blount Fine Foods chicken tortilla soup for wheat allergen
Misbranding, Unreported Allergens
- 2018-05-10CPSCTobi USA LLC., of Concord, Calif.Tobi Recalls Babynest Crib Bumpers Due to Strangulation Hazard; Sold Exclusively Online at babybay.us (Recall Alert)
The strings on the crib bumper exceed a safe length, posing a strangulation hazard to babies.
- 2018-05-10CPSCMunchkin Inc., of Van Nuys, Calif.Munchkin Recalls Waterpede Bath Toys Due to Choking Hazard
The bath toy can break apart exposing small parts, posing a choking hazard to young children.
- 2018-05-09FDA-FoodViable Solutions, LLCClass IMitragyna Speciosa Leaf Powder-Thai Maeng Da, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Thai Maeng Da***Origin: Thailand***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVA
Mitragyna Speciosa Leaf Powder Thai Maeng Da Kratom product is being recalled because they have the potential to be contaminated with Salmonella
- 2018-05-09FDA-FoodViable Solutions, LLCClass IMitragyna Speciosa Leaf Powder-GREEN Horn, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Green Horn***Origin: Indonesia***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children***2204 Cortland Place, Nampa, ID 83678***WWW.HERBAL-SALVATION.
Mitragyna Speciosa Leaf Powder Green Horn Kratom product is being recalled because they have the potential to be contaminated with Salmonella
- 2018-05-09FDA-FoodViable Solutions, LLCClass IMitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label is read in parts: "***herbal-salvation***Mitragyna Speciosa Leaf Powder Red Vein Sumatra***Origin: Indonesia***Disclaimer: This product is sold as a bulk botanical without directions or claims. Keep away from children**
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali Kratom products are being recalled because they have the potential to be contaminated with Salmonella
- 2018-05-09FDA-FoodTarget CorporationClass IIKidfresh Muy Cheesy Quesadillas 4.2oz UPC: 810882016057 Target item number: 270-2-955
Shipping container from CA to HI was not held at proper temperature which could cause food items to be contaminated with spoilage organisms or pathogens
- 2018-05-09FDA-FoodTarget CorporationClass IIMP NOVELTIES 12CT KIDS IC BARS UPC: 85239076101 Target item number: 288-7-2610
Shipping container from CA to HI was not held at proper temperature which could cause food items to be contaminated with spoilage organisms or pathogens
- 2018-05-09FDA-FoodTarget CorporationClass IIGREEN GIANT STEAMERS BABY BRUSSEL SPROUTS & BUTTER SAUCE 10OZ. UPC: 20000001401 Target item number 270-0-280
Shipping container from CA to HI was not held at proper temperature which could cause food items to be contaminated with spoilage organisms or pathogens
- 2018-05-09FDA-FoodIndependent Nutrition, Inc.Class IIgnite High Endurance Pre-Workout Supplement CAFFEINE FREE Formula, brand Wynant's Familty Health Foods, Net wt. 2.64 lbs. UPC 8 01650 01551 8. SAMPLE ONLY.
Ignite High Endurance Pre-Workout Supplement Caffeine Free dietary supplement product is recalled because label declared WHEY protein but do not declare milk.
- 2018-05-09FDA-FoodWysong CorporationClass IIProtein key brand Protein Meals varieties , 2.5 lb plastic container and 400 g plastic container, Varieties: Children's Plain
Wysong Corporation is conducting a voluntary recall of multiple varieties of Protein Key brand protein meals due to undeclared allergen soy.
- 2018-05-08CPSCHauck Fun For Kids, Inc., of Ontario, CanadaHauck Fun For Kids Recalls Go-Karts Due to Laceration and Collision Hazards
The steering wheel on the go-kart can detach, break or crack while in use, posing a laceration and/or collision hazard to young children.
- 2018-05-02CPSCThe William Carter Company, of Atlanta, Ga.Carter's Recalls Children's Cardigan Sets Due to Choking Hazard
The cardigan's toggle button can detach, posing a choking hazard to young children.
- 2018-04-19CPSCBase Brands LLC, of Atlanta, Ga.Base Brands Recalls Water Bottles Due to Violation of Lead Paint Standard (Recall Alert)
The pink paint on the outside of the bear water bottle contains levels of lead that exceed the federal lead paint standard. Lead is toxic if ingested by young children and can cause adverse health issues.
- 2018-04-19CPSCNingbo Tooky Toy Co. Ltd, of ChinaWild & Wolf Recalls Petit Collage Children's Toy Xylophones Due to Choking Hazard
The ball on the end of the toy xylophone beater stick can separate, posing a choking hazard to young children.
- 2018-04-18FDA-DeviceHamilton Medical AGClass IIHamilton-C3 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and neonates in the hospital.
After two and a half years, the battery fuel gauge may indicate a higher battery charge than what is available.
- 2018-04-18FDA-DeviceHamilton Medical AGClass IIHamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and neonates in the hospital.
After two and a half years, the battery fuel gauge may indicate a higher battery charge than what is available.
- 2018-04-18FDA-DeviceC.R. Bard, Inc.Class IIBard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube feeding, lavage fluid and medications Feeding Tubes with the ENFit(TM) Connector are made of a smooth plastic with a two-eyed tube used for nasogastric feeding of neonates, infants and adults as well as diagnostic and
BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.
- 2018-04-18FDA-DeviceC.R. Bard, Inc.Class IIBard(R) Adult/Pediatric Feeding Tube, ENFit(TM), REF EN0036420 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube feeding, lavage fluid and medications Feeding Tubes with the ENFit(TM) Connector are made of a smooth plastic with a two-eyed tube used for nasogastric feeding of neonates, infants and adults as well as diagnostic and t
BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.
- 2018-04-18FDA-DeviceC.R. Bard, Inc.Class IIBard(R) Infant Feeding Tube, ENFit(TM), REF EN0036410 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube feeding, lavage fluid and medications Feeding Tubes with the ENFit(TM) Connector are made of a smooth plastic with a two-eyed tube used for nasogastric feeding of neonates, infants and adults as well as diagnostic and therapeuti
BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.
Get notified about new baby recalls
Free weekly digest. We email when a new federal recall in this category — or anything else affecting your household — is published.
Get the Sunday Brief