Recalls: Personal Care

This recall involves Earthsonnets Wintergreen (Gualtheria procumbens) Essential Oil in a 10 mL amber bottle with a black continuous thread cap and euro-dropper. The label is blue and white with the firm's logo. Read more.

This recall involves NumbSkin pain relief cream with 5% lidocaine. The topical anesthetic cream was sold in 30 grams in a white with blue tube. NumbSkin is printed on the tube. Lot 9238 and a date code of 10/2019 through 09/2020 in a MM/YYYY format is embossed on the tub's thin end. Batch number 9238 is printed on the product packaging. Read more.

This recall involves sodium hydroxide and potassium hydroxide products that are sold in three sizes: 4 ounce, 8-ounce and 1-pound. The products are labeled as being used for soaps, cleaners, water treatment, food preparation, pH buffer and metal dissolution. The potassium hydroxide products and the 4-ounce and 8-ounce sodium hydroxide products are sold in black resealable bags; the 1-pound sodium hydroxide product is sold in a white resealable bag. The sodium hydroxide product is stated as being food grade. Read more.

This recall involves blister packages of prescription medications Sandimmune® (cyclosporine capsules, USP) 100 mg soft gelatin capsules and Neoral® (cyclosporine capsules, USP) MODIFIED 100 mg soft gelatin capsules from Novartis. Packages of Sandimmune 100 mg contain three blister cards with ten soft gelatin capsules per card and packages of Neoral 100 mg contain five blister cards with six soft gelatin capsules per card. The recalled blister packages have "Novartis," the name of the medication, dosage, NDC, lot number and expiration date on the outer package and on the blister cards. Only 100 mg doses of these medications with the following NDC and lot numbers and expiration dates are included in this recall: Recalled Prescription Drugs NDC Numbers Lot Numbers Expiration Date Sandimmune® (cyclosporine capsules, USP) 100 mg soft gelatin capsules 0078-0241-15 0078-0241-61 APCA136 APCA339 APCA793 APCC238 09/2020 02/2021 01/2022 07/2022 Neoral® (cyclosporine capsules, USP) MODIFIED 100 mg soft gelatin capsules 0078-0248-15 0078-0248-61 APCA437 APCA979 07/2020 03/2021 Read more.

This recall involves RESURRECTIONbeauty Wintergreen Essential Oil in amber glass 0.5-fluid-ounce dropper bottles. The bottles have a black cap and a green label with RESURRECTIONbeauty Wintergreen 100% Pure Essential Oil printed on the front. The UPC code 616913145877 is printed on the back of the product Read more.

This recall involves Airome Wintergreen 100% pure essential oils in 0.5- and 0.34-fluid-ounce amber glass dropper bottles sold without a child-resistant cap. It also includes Airome Deep Soothe 100% pure essential oils in 0.5-fluid-ounce amber glass dropper bottles sold without a child-resistant cap. Each bottle has a black cap and blue label with either "Airome Wintergreen 100% Pure Essential Oil Stimulate" or "Airome Deep Soothe 100% Pure Essential Oil Cool" printed on the front. A UPC code unique to each type of recalled bottle -83324503131, 833245034567, or 833245035977 - is printed on the bottom of the gift box in which the bottles were sold. The Arome Wintergreen 100% Pure Essential Oil Stimulate was sold separately and as part of a 3-pack "Focus & Concentrate Essential Oil Gift Set." Read more.

This recall involves the ALOCANE® Emergency Burn Pads (10 count and 15 count) which come in a white and red box with "MAXIMUM STRENGTH ALOCANE® Emergency Burn Pads" printed on the front. The product is an over the counter Gel Infused Pad with lidocaine (4%) as the active ingredient. The pads are sold in a 10 count box and 15 count box with the lot numbers 4179, 4180, 4235, 4645, 4646 or 4698 printed next to the barcode on the box. The UPC number for the affected product is 8-46241-02448-7 and can be found on the bottom of the box. Read more.

This recall includes all 10-, 30- and 60-mililiter amber glass bottles of wintergreen and birch essential oils sold prior to April 15, 2019. The label on each bottle displays the name of the product-Wintergreen or Birch-"100% Pure Therapeutic Grade Essential Oil," and the size of the container. Read more.

This recall involves bottles of prescription medications Losartan Potassium and Ezetimibe from Sandoz with certain lot numbers. The recalled bottles have "Sandoz," the name of the medication, dosage, and NDC on the front of the bottle labels and the lot number and expiration date on the side of the bottle labels. The recall includes the following: Recalled Prescription Drugs NDC Numbers Lot Numbers Expiration Date Ezetimibe 10mg Tablets 0781-5690-31 JE4491 Aug-2020 30 count bottle JE4492 Aug-2020 JE4493 Aug-2020 JE4495 Aug-2020 JG0308 Sep-2020 JG0310 Sep-2020 JG0311 Sep-2020 JG0312 Sep-2020 JG5061 Sep-2020 JG5063 Sep-2020 JK8921 Oct-2020 JK8922 Oct-2020 JK8923 Oct-2020 JK8924 Oct-2020 JL5535 Oct-2020 JM2253 Oct-2020 JM2254 Oct-2020 JM2255 Oct-2020 JM2257 Oct-2020 JM2258 Oct-2020 JM2259 Oct-2020 JM5986 Oct-2020 JM5987 Oct-2020 Ezetimibe 10mg Tablets 0781-5690-92 JE4481 Aug-2020 90 count bottle JG0249 Sep-2020 JK8989 Oct-2020 JN0764 Jan-2021 Losartan Potassium 50mg Tablets 0781-5701-31 HV9471 Feb-2020 30 count bottle Read more.

The recalled PipingRock wintergreen 100% pure essential oil is in a 1/2 fl. oz. (15 ml) glass amber dropper bottle. It has a black cap and a yellow, red and green label with PipingRock Wintergreen Oil Gaultheria procumbens 100% Pure Essential Oil printed on the front. Product number NT6446, UPC code 610256764467 and lot number 1905, 4000, 5980, 7420, 9344, 11202, 27180, 31397, 37913, 43369, 45843 or 56439 are printed on the back of the product. Read more.