Recalls: Other Containers and Packaging

October 16, 2025 Wilteexs Bioethanol Fuel Bottles Recalled Due to Risk of Serious Injury or Death from Flash Fire; Violates Mandatory Standards for Portable Fuel Containers and Hazardous Substances; Imported by Wilteexs

This recall involves Wilteexs-branded bottles of bioethanol used for tabletop fire pits, fireplaces, stoves and burners. The 1.06 quarts/1liter clear bottles come pre-filled with fuel. "WILTEEXS," "BIO ETHANOL" and an image of a burning flame are printed in blue and white on the front of the bottles. "X004IQ9ZCH" is printed below the barcode on the back of the bottles. Note: Recalled ethanol should be disposed of in accordance with any local and state regulations, contact your local hazardous waste treatment center or inquire about professional recycling points through the environmental protection agency. Do not dispose of ethanol in sewers, rainwater pipes or ordinary garbage cans to avoid causing fires or environmental pollution. Read more.


September 11, 2025 Blueroot Health Recalls Bottles of Bariatric Fusion Iron Multivitamins Due to Risk of Serious Injury or Death from Child Poisoning; Violates Mandatory Standard for Child-Resistant Packaging; Manufactured by VitaQuest International

This recall involves two types of Bariatric Fusion dietary supplement bottles: high ADEK multivitamin capsules (90 and 270-count bottles) and One Per Day bariatric multivitamin capsules (90-count bottle), both with 45mg of iron. The recalled bottles are white and orange. Only bottles with smooth cap tops that lack the "push down & turn" embossed lettering are included in this recall. The Bariatric Fusion logo is printed on the front of the bottles. Lot number 0066J4, 0065J4, 0453B5 or 0370B5 is printed on the bottom of the bottles. Read more.


November 22, 2023 Balloon Time Mini Helium Tanks Recalled by Worthington Industries Due to Injury Hazard

This recall involves Balloon Time Mini Helium Tanks that are used to fill up to 20 balloons with helium. They measure about 13.5 inches tall by 3.5 inches in diameter. The helium tanks have a red label and purple cap and hold 5.8 cubic feet of helium/air mixture. Read more.


January 19, 2023 Meguiar's Recalls Headlight Sealant Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning

This recall involves the Meguiar's Heavy Duty Headlight Sealant, which is included in the Meguiar's Heavy Duty Headlight Restoration Kit, product number G2980. The headlight sealant comes in a 2.5-ounce amber glass bottle and has "Headlight Sealant" in black lettering on a yellow background and "Heavy Duty" and "Meguiar's" printed on the label. Only headlight sealant packaged in an amber glass bottle are part of the recall. Read more.


November 3, 2022 FHS Retail Recalls FUUL Lamp Oil Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement; Poisoning Risk to Children

This recall involves FUUL 1.9L Pure Liquid Paraffin Lamp Oil products. The Lamp Oil is in a clear plastic bottle-like container with a square base and a white cap. The container label bears the brand "Fuul" followed by "Intense Heat", the product name "Liquid Paraffin Lamp Oil" and the descriptors "Pure, Colorless, Smokeless" and "1.9 Liter (.5 Gallons)". The label includes the warning, "Product contains petroleum distillates. Harmful or fatal if swallowed. KEEP OUT OF REACH of children or pets." Read more.


June 30, 2022 Mohnark Pharmaceuticals Recalls Lidocaine Topical Anesthetic Cream Due to Failure to Meet Child-Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

The recall involves Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream. The product was sold in a white tube with a flip-top closure. Mohnark Pharmaceuticals is printed under the blue and green logo on the right side of the product tube. The lot code is located at the bottom of the product tube. The affected lot codes are 01202201, 210201, 210301, 210503, 210505, 210601, 211002 and 210401. The UPC 860002324906 is located on bottom side panel of the packaging. Read more.


April 14, 2022 Rae Wellness Recalls Prenatal and Immunity Dietary Supplements Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves bottles of Rae Wellness Prenatal and Immunity Capsules. Both products were sold in 60-capsule bottles and contain iron and have "Rae" in yellow lettering and "Prenatal" or "Immunity" printed on the label. The bottles have a white continuous thread closure. Read more.


April 7, 2022 biOrigins Sodium Hydroxide Products Recalled Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement; Imported by Madar Corporation; Sold Exclusively at Amazon.com (Recall Alert)

The recall involves biOrigins-branded sodium hydroxide products. The product was sold in 500 grams and 1-kilogram zip-top, silver bags. The biOrigins logo and "LYE CAUSTIC SODA/SODIUM HYDROXIDE" are printed on the front of the bag on a white and blue label. The weight and batch number 4430708, 4423901, 4415403 or 4408414 appear on the back of the product. Read more.


March 17, 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)

This recall involves the PhysiciansCare brand Extra Strength Non Aspirin, Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack over-the-counter drugs. The products contain aspirin, acetaminophen, or ibuprofen. They are packaged in cardboard boxes of 50, 100, 250, and 500 tablets per box. Product Drug Tablet Amount Extra Strength Non Aspirin Acetaminophen (500 mg) 50 tablets 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Aspirin Aspirin (325 mg) 50 tablets 100 tablets 250 tablets 500 tablets Extra Strength Pain Reliever Acetaminophen (250 mg) Aspirin (250 mg) 100 tablets 250 tablets Ibuprofen Ibuprofen (200 mg) 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Medication Station / Multi-Pack Acetaminophen (500 mg) Aspirin (325 mg) Ibuprofen (200 mg) Antacid (420 mg) 4 boxes of 100 tablets each with outer station 4 boxes of 100 tablets each without outer station The Antacid is not subject to this recall. Read more.


July 1, 2021 TBD Liquids Recalls Liquid Nicotine Products Due to Failure to Meet Child-Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

This recall involves "The Best Damn Liquids" branded liquid nicotine products in all flavors packaged in clear plastic bottles in 120 mL and 240 mL sizes with a continuously threaded closure. Read more.