Belle Chemical Recalls Sodium Hydroxide and Potassium Hydroxide Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement

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The products contain sodium hydroxide or potassium hydroxide 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 chemical burns and irritation to the skin and eyes. In addition, the label on the product violates the Federal Hazardous Substance Act (FHSA) by omitting the word “poison” for poisonous chemicals and the mandatory hazard statement on the front on the packaging.

Source: Recall List

Earth Sonnets Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

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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.

Source: Recall List

Belle Chemical Recalls Drain Cleaner Product Due to Violation of FHSA Labeling Requirement

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The product contains sodium hydroxide.  The label on the product violates the Federal Hazardous Substance Act (FHSA) by omitting the word “poison” for poisonous chemicals and the mandatory hazard statement on the front on the packaging.

Source: Recall List

Boyer Recalls Six Brands of Sodium and Potassium Hydroxide Due to Failure to Meet Child-Resistant Packaging Requirement; Injuries Reported

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The products contain sodium and/or potassium hydroxide 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 chemical burns and irritation to the skin and eyes.

Source: Recall List

Earthroma Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

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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.

Source: Recall List

NumbSkin Pain Relief Cream Recalled by SeeNext Venture Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

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The packaging is not child resistant as required by the Poison Prevention Packaging Act.  The pain relieving cream contains lidocaine, posing a risk of poisoning to young children if they put it on their skin or ingest it.

Source: Recall List

American Honda Recall of Portable Generators Due to Fire and Burn Hazards

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The portable generator’s inverter assembly can short circuit with the presence of salt water. This causes the unit to smoke or catch fire, posing fire and burn hazards to consumers.

Source: Recall List

Chicago Indoor Garden Voluntarily Recalls Clover Sprouts and Prducts containing Clover Sprouts Due To Possible Health Risk

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It has been brought to our attention by the FDA that products containing Red Clover sprouts purchased with the "Best By" dates between 12/1/19 through 3/12/20 may have been contaminated with E. coli0103. At this time no illnesses have been reported

Source: Food and Drugs Administration--Recalls/Safety Alerts

Chicago Indoor Garden Voluntarily Recalls Clover Sprouts and Products Containing Clover Sprouts Due To Possible Health Risk

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It has been brought to our attention by the FDA that products containing Red Clover sprouts purchased with the "Best By" dates between 12/1/19 through 3/12/20 may have been contaminated with E. coli0103. At this time no illnesses have been reported

Source: FDA Food Safety Recalls RSS Feed

Natural Remedy Store Issues Voluntary Worldwide – Recall of Active Male Due to Presence of Undeclared Tadalafil

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Natural Remedy Store is voluntarily recalling all lots of Active Male, 500mg capsules to the consumer level. FDA analysis has found the product to be tainted with undeclared tadalafil

Source: Food and Drugs Administration--Recalls/Safety Alerts