Drug Recall: Sandoz Aprepitant Caps, Lidocaine/Prilocaine Cream

Drug Recall: Sandoz Aprepitant Caps, Lidocaine/Prilocaine Cream

Click to enlarge

US FlagUS/Washington: Sandoz Inc., a Princeton, New Jersey establishment, recalls an estimated 156,750 Aprepitant Capsules and Lidocaine/Prilocaine Cream from the American marketplace due to 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://bit.ly/423xRw3

Direct link: https://www.cpsc.gov/Recalls/2023/Sandoz-Recalls-Aprepitant-Capsules-and-Lidocaine-and-Prilocaine-Cream-Prescription-Drugs-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Aprepitant Capsules and Lidocaine and Prilocaine Cream products marketed, sold and delivered in the United States, as follows:

Continue reading

Walgreens Acetaminophen Arthritis Pain Reliever [US]

Walgreens Acetaminophen Arthritis Pain Reliever [US]

Click to enlarge

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:

Continue reading

Kroger Aspirin & Ibuprofen Pain Reliever [US]

Kroger Aspirin & Ibuprofen Pain Reliever [US]

Click to enlarge

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:

Continue reading

Walgreens Acetaminophen Pain Reliever [US]

Walgreens Pain Reliever Acetaminophen [US]

Click to enlarge

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:

Continue reading

Drug Recall: Best Naturals Organic Wintergreen Essential Oil

Best Naturals Organic Wintergreen Essential Oil [US]

Click to enlarge

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:

Continue reading

Telebrands Hempvana Pain Relief Creme [US]

Telebrands Hempvana Pain Relief Creme [US]

Click to enlarge

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:

Continue reading

Rae Prenatal Capsules & Rae Immunity Supplements [US]

Rae Prenatal Capsules & Rae Immunity Capsules [US]

Click to enlarge image

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:

Continue reading

PhysiciansCare Aspirin & Ibuprofen Pain Relievers [US]

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

Click to enlarge image

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:

Continue reading

TBD Liquid Nicotine Recall [US]

TBD branded Liquid Nicotine Products

Click to enlarge

US FlagUS/Washington: TBD Liquids LLC, a Santa Rosa, California establishment, recalls all current batch/lots (estimated to be 1,000 bottles) of TBD branded Liquid Nicotine products from the American marketplace due to reported failure to meet US child resistant closure requirements under the US Poison Prevention Packaging Act and consequential risks of child poisoning, drug overdose, ingestion and GI tract laceration damage, all serious health and safety hazards.

CPSC: http://ht.ly/tKAD30rMLk0

Direct link: https://www.cpsc.gov/Recalls/2021/TBD-Liquids-Recalls-Liquid-Nicotine-Products-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain TBD branded Liquid Nicotine Products, as follows:

Continue reading

Pro Supply Outlet Sodium, Potassium Hydroxide Recall [US]

Pro Supply Outlet Sodium, Potassium Hydroxide Recall [US]

Click to enlarge image

US FlagUS/Washington: Chemical Technologies International Inc., doing business as Pro Supply Outlet, a Rancho Cordova, California establishment, recalls an estimated 2,600 canisters of Pro Supply Outlet (“PSO”) branded Potassium Hydroxide and Sodium Hydroxide chemical products from the American marketplace due to reported 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/cb0J30rM9Je

Direct link: https://www.cpsc.gov/Recalls/2021/Pro-Supply-Outlet-Recalls-Sodium-and-Potassium-Hydroxide-Products-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-and-Violation-of-FHSA-Labeling-Requirement-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain consumer-grade Potassium Hydroxide and Sodium Hydroxide products, as follows:

Continue reading

Plant Guru Wintergreen & Birch Essential Oil Recall [US]

Plant Guru Essential Oil Recall [US]

Click to enlarge image

US FlagUS/Washington: Plant Guru, a Plainfield, New Jersey establishment, recalls an estimated 25,600 bottles of Wintergreen Essential Oil, Birch Essential Oil, Headache Relief Essential Oil Blend, Headache Relief Roll-On Essential Oil Blend and Deep Muscle Essential Oil Blend 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/U8mC30rLNem

Direct link: https://www.cpsc.gov/Recalls/2021/Plant-Guru-Recalls-Wintergreen-Birch-and-Blends-of-Essential-Oils-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 certain bottles of Plant Guru Essential Oils, as follows:

Continue reading

LifeSeasons Blood Nourish-R Supplement Recall [US]

LifeSeasons Blood Nourish-R Supplement Recall [US]

Click to enlarge

US FlagUS/Washington: LifeSeasons Inc., a Springville, Utah establishment, recalls an estimated 7,800 bottles of LifeSeasons Blood Nourish-R Supplements 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/I2l030rLH8e

Direct link: https://www.cpsc.gov/Recalls/2021/UST-Recalls-Bottles-of-LifeSeasons-Blood-Nourish-R-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain LifeSeasons Blood Nourish-R Supplements marketed, sold and delivered in the United States, as follows:

Continue reading

The Lye Guy Potassium, Sodium Hydroxide Recall [US]

The Lye Guy Sodium Hydroxide and Potassium Hydroxide Recall [US]

Click to enlarge

US FlagUS/Washington: The Lye Guy, a Pennellville, New York establishment, recalls an estimated 32,000 canisters of Potassium Hydroxide and Sodium Hydroxide chemical products from the American marketplace due to reported 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/xOQH30rL6Wz

Direct link: https://www.cpsc.gov/Recalls/2021/The-Lye-Guy-Recalls-Sodium-and-Potassium-Hydroxide-Products-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-and-Violation-of-FHSA-Labeling-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves certain consumer-grade The Lye Guy Potassium Hydroxide and Sodium Hydroxide products, as follows:

Continue reading

Welmate Lidocaine Numbing Cream Recall [US]

Welmate Lidocaine Numbing Cream Recall [US]

Click to enlarge image

US FlagUS/Washington: YYBA Corp., doing business as Wellspring, a Monsey, New York establishment, recalls an estimated 15,000 jars of Welmate Lidocaine Numbing Cream from the American marketplace due to 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/DH9A30rGou9

Direct link: https://www.cpsc.gov/Recalls/2021/YYBA-Recalls-Welmate-Lidocaine-Numbing-Cream-Due-to-Failure-to-Meet-Child-Resistant-Packaging-Requirement-Risk-of-Poisoning-Recall-Alert

Additional information:
The US Consumer Product Safety Commission (“CPSC”) reports this recall involves Welmate Lidocaine Numbing Cream marketed, sold and delivered in the United States, as follows:

Continue reading

dōTERRA Deep Blue & PastTense Essential Oil Recall [US]

dōTERRA Deep Blue & PastTense Essential Oil Recall [US]

Click to enlarge

US FlagUS/Washington: dōTERRA International LLC, a Pleasant Grove, Utah establishment, recalls an estimated 1.3 million Deep Blue, PastTense and Deep Blue Touch branded Essential Oil 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: http://ht.ly/H6CC30rFXd8

Direct link: https://www.cpsc.gov/Recalls/2021/doTERRA-Recalls-1-3-Million-Bottles-of-Deep-Blue-PastTense-and-Deep-Blue-Touch-Essential-Oils-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 certain dōTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils in 10 mL glass bottles with rollerball applicator and black cap, as follows:

Continue reading