Recalls: Personal Care

May 14, 2020 Organic Pure Oil Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold Exclusively on Amazon.com (Recall Alert)

This recall involves 4 fl. oz (118 mL) amber glass bottles with black dropper cap of Organic Pure Oil Wintergreen Essential Oil. The green and pink label on each bottle displays "Organic Pure Oil," "Wintergreen", "Gaultheria Procumbens." The volume amount of the bottle is printed on the label. The Organic Pure Oil logo and product name are printed in green. UPC code 731525205594 can be found in the online listing for the product. Read more.


April 23, 2020 LUS Recalls Hair Dryers Due to Electrocution or Shock Hazard (Recall Alert)

This recall involves the LUS Dryer & Diffuser. The handheld hair dryers were sold in white, in a box that also contains a diffuser. The hair dryers have the model number HD-LUS01 printed under the back end of the hair dryer. The logos "LUS Brands" and "Love Ur Curls" are located on either side of the back end of the dryer. Read more.


March 18, 2020 Novartis Recalls 100 mg Sandimmune and Neoral Prescription Drug Blister Packages Due to Failure to Meet Child-Resistant Packaging Requirement; Risk of Poisoning

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.


March 18, 2020 Belle Chemical Recalls Sodium Hydroxide and Potassium Hydroxide Products Due to Failure to Meet Child-Resistant Packaging Requirement and Violation of FHSA Labeling Requirement

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.


March 18, 2020 Earthroma Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

This recall involves Earthroma's Wintergreen Essential oil in amber bottles of 5 mL, 15 mL, and 30 mL. The products include a green and white label with the firm's logo. Read more.


March 18, 2020 NumbSkin Pain Relief Cream Recalled by SeeNext Venture Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

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.


March 18, 2020 Earth Sonnets Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

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.


November 21, 2019 RESURRECTIONbeauty Recalls Wintergreen Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

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.


November 20, 2019 B&B Acquisition Recalls Wintergreen Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning

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.


November 14, 2019 Quest Products Recalls ALOCANE Emergency Burn Pads Due to Failure to Meet Child Resistant Closure Requirement; Risk of Poisoning

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.