Product Recall: Blue’s Clues Foot to Floor Ride-on Toys

Product Recall: Blue's Clues Foot to Floor Ride-on Toys

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US FlagUS/Bethesda: Huffy Corporation, a Miamisburg, Ohio establishment, recalls an estimated 28,550 Blue’s Clues Foot to Floor Ride-on Toys from the American marketplace due to suspected in-use balance failure and consequential risks of falls, laceration, traumatic brain injury (“TBI” or “concussion”), bone fractures and/or central nervous system (“CNS”) injury, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CPSC: https://bit.ly/3Bvmzp6

Direct link: https://www.cpsc.gov/Recalls/2022/Huffy-Corporation-Recalls-Ride-On-Toys-Due-to-Fall-and-Injury-Hazards

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Blue’s Clues Foot to Floor Ride-on Toys, as follows:

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Product Recall: Jack & Milly Koala Children’s Sippy Cups

Jack & Milly Koala Children's Sippy Cups Recall [Australia]

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Australia FlagAustralia/Canberra: Myer Pty Ltd, a Melbourne, Victoria establishment, recalls certain batch/lots of Jack & Milly Koala Children’s Sippy Cups from the Australian marketplace due to reported component detachment and consequential risks of choking, oral injury, internal ingestion, GI tract laceration damage, bowel obstruction and/or sepsis, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

ACCC: https://bit.ly/3NnW7AE

Direct link: https://www.productsafety.gov.au/recalls/myer-pty-ltd-%E2%80%94-jack-milly-koala-sippy-cup

Additional information:
The Australian Competition & Consumer Commission (“ACCC”) reports the following Children’s Sippy Cups are subject to this recall:

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Walgreens Acetaminophen Arthritis Pain Reliever [US]

Walgreens Acetaminophen Arthritis Pain Reliever [US]

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US FlagUS/Washington: Walgreen Co., a Deerfield, Illinois establishment, recalls an estimated 25,660 bottles of Walgreens branded Acetaminophen Arthritis Pain Acetaminophen Pain Reliever from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CPSC: https://cutt.ly/DKjPNKT

Direct link: https://www.cpsc.gov/Recalls/2022/Aurohealth-Recalls-Kroger-Brand-Acetaminophen-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-%20Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain batch/lots of Acetaminophen Arthritis Pain Reliever products, as follows:

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Kroger Aspirin & Ibuprofen Pain Reliever [US]

Kroger Aspirin & Ibuprofen Pain Reliever [US]

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US FlagUS/Washington: Time-Cap Labs Inc., a Farmingdale, New York establishment, recalls an estimated 209,430 bottles of Kroger branded Aspirin and Kroger branded Ibuprofen Pain Reliever products from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: https://cutt.ly/AKozfP3

Direct link: https://www.cpsc.gov/Recalls/2022/Time-Cap-Labs-Recalls-Kroger-Brand-Aspirin-and-Ibuprofen-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain batch/lots of Kroger branded Aspirin and Ibuprofen Pain Reliever products, as follows:

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Walgreens Acetaminophen Pain Reliever [US]

Walgreens Pain Reliever Acetaminophen [US]

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US FlagUS/Washington: Walgreen Co., a Deerfield, Illinois establishment, recalls an estimated 137,300 bottles of Walgreens branded Acetaminophen Pain Reliever from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: https://cutt.ly/aKtClC8

Direct link: https://www.cpsc.gov/Recalls/2022/Aurohealth-Recalls-Walgreens-Brand-Acetaminophen-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain batch/lots of Acetaminophen Pain Reliever products, as follows:

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Asweets Global Wonder & Wise Baby Activity Walkers [US]

Asweets Global Wonder & Wise Baby Activity Walkers [US]

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US FlagUS/Bethesda: Asweets Global Inc., a City of Industry, California establishment, recalls an estimated 13,300 Wonder & Wise Baby Activity Walkers from the American marketplace due to suspected component detachment and consequential risks of choking, oral injury, internal ingestion, GI tract laceration damage, bowel obstruction and/or sepsis, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CPSC: https://cutt.ly/TJn4SHs

Direct link: https://www.cpsc.gov/Recalls/2022/Asweets-Recalls-Wood-Baby-Activity-Push-Walkers-Due-to-Strangulation-Hazard

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves four-wheeled Wonder & Wise Baby Activity Walkers marketed, sold and delivered in the United States, as follows:

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Drug Recall: Best Naturals Organic Wintergreen Essential Oil

Best Naturals Organic Wintergreen Essential Oil [US]

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US FlagUS/Washington: Best Nutritionals LLC, a Piscataway, New Jersey establishment, recalls an estimated 2,800 Best Naturals Organic Wintergreen Essential Oils from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/kKlF30sjnkR

Direct link: https://www.cpsc.gov/Recalls/2022/Best-Nutritionals-Recalls-Organic-Wintergreen-Essential-Oil-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirements-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain batch/lots of Organic Wintergreen Essential Oil products, as follows:

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FAO Schwarz Wooden Toys [US]

FAO Schwarz Wooden Toys [US]

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US FlagUS/Bethesda: MerchSource LLC, an Irvine, California establishment, recalls an estimated 46,200 FAO Schwarz branded Toys (26,400 FAO Schwarz branded Toy Wood Play Smart Robot Buddy Toys and 19,800 FAO Schwarz branded Toy Wood Sensory Boards) from the American marketplace due to suspected component detachment and consequential risks of choking, oral injury, internal ingestion, GI tract laceration damage, bowel obstruction and/or sepsis, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CPSC: http://ht.ly/huFv30shKSE

Direct link: https://www.cpsc.gov/Recalls/2022/MerchSource-Recalls-FAO-Schwarz-Branded-Toy-Wood-Play-Smart-Robot-Buddys-and-Wood-Sensory-Boards-Due-to-Choking-Hazard

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain FAO Schwarz branded Toy Wood Play Smart Robot Buddy and the Toy Wood Sensory Board marketed, sold and delivered in the United States, as follows:

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Telebrands Hempvana Pain Relief Creme [US]

Telebrands Hempvana Pain Relief Creme [US]

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US FlagUS/Bethesda: Telebrands Corp., a Fairfield, New Jersey establishment, recalls an estimated 183,000 Telebrands Hempvana Pain Relief Products with Lidocaine from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/woWq30shwLO

Direct link: https://www.cpsc.gov/Recalls/2022/Telebrands-Recalls-Hempvana-Pain-Relief-Products-with-Lidocaine-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves Telebrands Hempvana Pain Relief Products products, as follows:

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Rae Prenatal Capsules & Rae Immunity Supplements [US]

Rae Prenatal Capsules & Rae Immunity Capsules [US]

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US FlagUS/Bethesda: Rae Wellness, a Minneapolis, Minnesota establishment, recalls an estimated 191,200 Rae Prenatal Capsules and Rae Immunity Capsules from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/Mbns30shmsM

Direct link: https://www.cpsc.gov/Recalls/2022/Rae-Wellness-Recalls-Prenatal-and-Immunity-Dietary-Supplements-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves Rae Nutritional Supplement products, as follows:

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Helix Metal Lockable Drug Chests [US]

Helix Metal Lockable Drug Chests Recall [US]

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US FlagUS/Washington: Maped Helix USA Inc., a Bloomingdale, Illinois establishment, recalls an estimated 7,700 Helix Metal Lockable Drug Chests from the American marketplace due to suspected operational locking failure and consequential risks of unauthorized drug access, poisoning, overdose, oral injury, internal ingestion, GI tract laceration damage, bowel obstruction and/or sepsis, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CPSC: http://ht.ly/H5n830sh7qM

Direct link: https://www.cpsc.gov/Recalls/2022/Maped-Helix-USA-Recalls-Metal-Lockable-Drug-Chests-Due-to-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Helix Metal Lockable Drug Chests marketed, sold and delivered in the United States, as follows:

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PhysiciansCare Aspirin & Ibuprofen Pain Relievers [US]

15613 - CPSC - PhysiciansCare Aspirin & Ibuprofen Pain Relievers [US]

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US FlagUS/Washington: Acme United, a Rocky Mount, North Carolina and a Vancouver, Washington establishment, recalls an estimated 165,000 units of PhysiciansCare branded Aspirin, PhysiciansCare branded Extra Strength Non Aspirin, PhysiciansCare branded Extra Strength Pain Reliever, PhysiciansCare branded Ibuprofen, PhysiciansCare branded Medication Station, and PhysiciansCare branded Drug Multi-Pack from the American marketplace due to suspected failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/4qQH30sfnAH

Direct link: https://www.cpsc.gov/Recalls/2022/Acme-United-Corporation-Recalls-PhysiciansCare-Brand-Over-the-Counter-Drugs-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
US Consumer Product Safety Commission (“CPSC”) reports this recall involves multiple SKUs of PhysiciansCare Pain Relief products, as follows:

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DigitDots Magnetic Ball Toys [US]

DigitDots Magnetic Ball Recall [US]

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US FlagUS/Washington: HD Premier Inc., a Wilmington, Delaware establishment, recalls an estimated 119,620 DigitDots branded 3 mm and 5 mm sized Magnetic Ball Toys from the American marketplace due to suspected risks of accidental ingestion with consequential choking, oral injury, internal ingestion, GI tract laceration damage, bowel obstruction and perforations, twisting and/or blockage of the intestines, infection, blood poisoning, sepsis and/or death, all serious health and safety hazards requiring immediate medical intervention to minimize suffering and prevent life-changing injury.

CPSC: http://ht.ly/MXg130seEZg

Direct link: https://www.cpsc.gov/Recalls/2022/HD-Premier-Recalls-DigitDots-Magnetic-Balls-Due-to-Ingestion-Hazard

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain DigitDots Magnet Toys marketed, sold and delivered in the United States, as follows:

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Zeno Wheeled Infant Walkers [US]

Zeno Wheeled Infant Walker Recall [US]

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US FlagUS/Washington: Zeno Inc., a Weymouth, Massachusetts establishment, recalls an estimated 1,355 Zeno Wheeled Infant Walkers from the American marketplace due to suspected failure to comply with Federal Safety Standards for Infant Accessories and consequential risks of unauthorized travel, falls, laceration, entrapment, traumatic brain injury (“TBI” or “concussion”), bone fractures and/or central nervous system (“CNS”) injury, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CPSC: http://ht.ly/G7qK30sc1wQ

Direct link: https://www.cpsc.gov/Recalls/2022/Zeno-Recalls-Infant-Walkers-Due-to-Fall-and-Entrapment-Hazards-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain Zeno Collapsible Infant Walkers with adjustable height settings marketed, sold and delivered in the United States, as follows:

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Abbott Similac Baby Food [Canada]

Abbott Similac Baby Food Recall [Canada]

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Canada FlagCanada/Ottawa: Abbott Nutrition, a Saint-Laurent, Québec establishment, recalls certain batch/lots of Similac Baby Food from the Canadian marketplace due to suspected Cronobacter sakazakii and Salmonella contamination and consequential risks of Gram-negative bacterial infection, severe illness and/or possible life-changing complications, all serious health and safety hazards requiring immediate medical intervention to minimize pain and suffering as well as prevent life-altering injury or death.

CFIA: http://ht.ly/6O2g30sbcgT

Direct link: https://recalls-rappels.canada.ca/en/alert-recall/certain-abbott-brand-powdered-infant-formula-products-recalled-due-cronobacter#wb-auto-23

Additional information:
The Canadian Food Inspection Agency (“CFIA”) reports the following Infant Formula products are subject to this recall:

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