Recalls: Containers and Packaging

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.

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.

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.

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.

This recall involves Aesop Post-Poo Drops, a bathroom deodorizer in a 100 mL amber glass bottle, with a continuous thread pipette dispenser closure. The bottle has a black and cream label with the brand name Aesop. The UPC number 9319944009200 is located on the rear of the bottle, directly below the ingredients list. The deodorizer product was also sold in four versions of the Home Kit: The Protector, The Seasoned Wayfarer, The Melodist, and The Familiar Horizon. The UPC numbers for four versions of the Home Kit are located on the rear of the printed sleeve. Only the Aesop Post-Poo Drops in the kit are included in this recall. The product names and UPC are as follows: Product Name UPC Description Post-Poo Drops 9319944009200 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Protector 9319944030198 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Seasoned Wayfarer 9319944023794 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Melodist 9319944022278 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Familiar Horizon 9319944016017 100 mL amber glass bottle, with a continuous thread pipette dispenser closure. This recall also involves four Aesop Oil Burner Blends: Anouk, Beatrice, Catherine, and Isabelle. The aromatic oil blends intended to be used in an oil burner. These products include a black and cream label with the brand name Aesop and the blend name. They come in a 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert. The UPC numbers for the Oil Burner Blends are located on the rear of each bottle, below the ingredients lists. The product names and UPC for the recalled Oil Burner Blend products are as follows: Product Name UPC Description Anouk Oil Burner Blend 9319944000696 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Beatrice Oil Burner Blend 9319944000702 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Catherine Oil Burner Blend 9319944000689 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Isabelle Oil Burner Blend 9319944016871 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Read more.

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.

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.

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.

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.

This recall involves the Kroger brand aspirin and ibuprofen over-the-counter drugs. For the aspirin product, the green and yellow label states Kroger, Low Dose, Aspirin, 81 mg Delayed-Release Tablets / Pain Reliever, 300 enteric coated tablets. The bottle has a green continuous thread gear closure. For the ibuprofen product, the blue and white label states Kroger, Ibuprofen, Capsules, 200 mg Pain Reliever / Fever Reducer, 160 softgels. The bottle has a blue continuous thread gear closure. The following UPC and Lot numbers listed in the table are included in this recall and can be found on the label on the back of the bottle. Item UPC Lot numbers Aspirin 4126001295 A077J F032H F035H J011H K031H Ibuprofen 4126001298 FH1163 C11044 C11047 C11064 C11065 C11079 C11084 Read more.