Recalls: Containers and Packaging

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 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 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 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.

This recall involves Best Naturals Organic Wintergreen Essential oil in dark amber glass bottles with a black continuous thread closure. The product was sold in 4 fl oz. "Organic Wintergreen Essential Oil" and the firm's logo is printed on the green and orange label. The UPC 817716016719 is printed on the back side of the label. Read more.

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.

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.

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.