Recalls: Containers and Packaging

May 25, 2023 The Good and the Beautiful Recalls Math 1 and Math 3 Boxes Due to Laceration Hazard (Recall Alert)

This recall involves The Good and the Beautiful Math 1 and Math 3 boxes with metallic whiteboards. The boxes include lids with attached metallic whiteboards and labeled Math 1 or Math 3 on the lids, bottom, left side and right side. The Math 1 Box measures about 9 inches square and the Math 3 Box measures about 7 inches square. Read more.


May 18, 2023 Acme United Recalls PhysiciansCare Brand Allergy Relief and Cold and Cough Tablets Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold on Amazon.com

This recall involves PhysiciansCare brand Allergy caplets with item number 90036, Allergy Plus tablets with item number 90091, and Cold and Cough tablets with item numbers 90092 and 90033. They are packaged in boxes of 50, 100 and 250 tablets/caplets. The item numbers are printed on the top right corner of the box. The recall includes the following: Item Number Description 90036 PhysiciansCare Allergy; 50 caplets 90091 PhysiciansCare Allergy Plus; 100 tablets Non-Drowsy Cold and Cough; 100 tablets 90033 PhysiciansCare Cold and Cough; 250 tablets Read more.


March 9, 2023 Sandoz Recalls Aprepitant Capsules and Lidocaine and Prilocaine Cream Prescription Drugs Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves prescription drugs Aprepitant 125 mg capsules sold in cartons containing one blister card of 6 capsules and 5 gram tubes of Lidocaine and Prilocaine cream sold in cartons containing 5 tubes and packed with or without 12 dressings. The Aprepitant capsules are in a non-child resistant blister card packaged in a carton that has the name "Sandoz," the name of the medication, dosage, NDC number, lot number, and expiration date on the carton and on the blister cards. The warnings "This unit-dose packaging is not child-resistant" and "For institutional use only" are listed on the carton. The Lidocaine and Prilocaine cream is packaged in a 5 gram tube with a continuous thread white closure. The name "fougera®," the name of the medication, dosage and NDC number are printed on the carton and tube and the expiration date and lot number are printed on the carton and stamped on the crimp of the tube. The warning "FOR HOSPITAL USE ONLY" is printed on the carton and the tube. Product Description NDC Number Lot Number Expiration Date Aprepitant Capsules 125 mg 0781-2323-68 Carton of 1 Blister Pack of 6 capsules 0781-2323-06 Blister Pack LK3209 LC6454 04/2024 12/2023 Lidocaine and Prilocaine 2.5%/2.5% Cream 5 gram Tubes 0168-0357-56 Carton of 5 tubes and 12 dressings 0168-0357-55 Carton of 5 tubes 0168-0357-05 Tube LA2782 LA2784 LV0667 LX5350 MA1640 MB3205 LA2785 LR9041 MB3209 03/2023 03/2023 02/2024 03/2024 03/2024 04/2024 03/2023 11/2023 04/2024 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.


September 8, 2022 Roots & Harvest Wide Mouth Pint Canning Jars Recalled by LEM Products Distribution Due to Laceration Hazard

This recall involves Wide Mouth Pint Canning Jars that were sold in 12-packs in a cardboard sleeve shrink wrapped in clear plastic. The jars are clear glass with the Roots & Harvest brand molded on each jar. The jars have a metal lid and screw on type band. These jars are used for canning food. 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.


June 16, 2022 Aurohealth Recalls Kroger Brand Acetaminophen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves the Kroger brand acetaminophen. The red, white, and yellow label states, Kroger, Acetaminophen, Arthritis Pain, Extended-Release, Tablets USP, 650 mg, 225 extended-release tablets. The bottle has a red continuous thread gear closure. UPC number 041260012846 and lot numbers P2100890, P2100891, P2100992 (each with expiration date Aug-2023) and P2101010 (with expiration date Apr-2023) are included in this recall. The UPC number, lot number and expiration date are printed near the drug facts panel on the label on the back of the bottle. Read more.


June 16, 2022 Sun Pharma Recalls Kroger Brand Acetaminophen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves the Kroger brand acetaminophen over-the-counter drug. The red, white and gray label states Kroger, Acetaminophen, Extended-Release Tablets USP, 650mg, Pain Reliever/Fever Reducer, 100 caplets. The bottle has a white continuous thread closure. The UPC number is 041260012877 with the batch codes AC45463, AC38213 or AC30682. The location of the UPC number is under the bar code on the packaging and the batch code is at the bottom of the label on the bottle. Read more.


June 16, 2022 Aurohealth Recalls Walgreens Brand Acetaminophen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves the Walgreens brand acetaminophen product. The red and white label states Walgreens, Easy Open for Adults, Pain Reliever, Acetaminophen, 500 mg, Fever Reducer, Extra Strength, 150 caplets. The bottle has a red continuous thread gear closure. UPC number 311917218090 and Lot numbers P2100627, P2100671, P2100672, P2100689 P2100747, P2100859 (each with expiration date Nov-2022) and P2200050 (with expiration date Jan-2023) are included in this recall. The UPC number, lot numbers and expiration date are printed near the drug facts panel on the label on the back of the bottle. Read more.