Recalls: Other Containers and Packaging

April 16, 2020 Dr. Adorable Recalls Sweet Birch Essential Oil Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning; Sold Exclusively on Amazon.com (Recall Alert)

This recall involves 4.4 fl. oz. (144 mL) and 8 fl. oz. (240 mL) plastic amber bottles with white flip top lids. The white oval label on the bottle displays the Dr. Adorable logo, product name and the volume amount of the bottle. Read more.


April 16, 2020 The Vitamin Shoppe Recalls Energy Formula Multivitamins Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning (Recall Alert)

This recall involves The Vitamin Shoppe's Energy Formula multivitamins in a white bottle with a blue, white, and gold label. Each bottle contains 90 tablets and has the code VS-3293 with the lot number 8102351 located on the bottom of the bottle. Read more.


April 16, 2020 Wyndmere Naturals Recalls Birch Sweet Essential Oil and Aches & Pains Synergistic Essential Oil Blend Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning

This recall involves Birch Sweet Essential Oil in a 10 mL cobalt blue glass bottle with a black cap and a yellow label. "Wyndmere," "Birch Sweet," "Pure Essential Oil," and UPC code 602444000907 are printed on the label. The batch number 12717-65 is printed on the bottom of the bottle in yellow ink. The Aches & Pains Synergistic Blend was sold in a 10 mL cobalt blue glass bottle with a black cap and blue label. "Wyndmere," "Aches & Pains," "Synergistic Blend," and UPC code 602444010609 are printed on the label. Batch number 112019-65 is printed on the bottom of the bottle in yellow ink. 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 Boyer Recalls Six Brands of Sodium and Potassium Hydroxide Due to Failure to Meet Child-Resistant Packaging Requirement; Injuries Reported

This recall involves six brands of sodium and potassium hydroxide products sold in two pound clear plastic bottles with a continuous thread closure cap. The products are commonly advertised as being used for home soapmaking projects and clearing drains. The lot numbers included in the recall are from 4001 to 9288 and are located on the bottom of the jar and on the side of the box. The brands of products and description of the packaging included in the recall are: Brand Description Distributed By Soap Supply Co. Lye yellow label BigTProducts Soap Makers Lye green label BigTProducts California Soap Supply dark blue label NG Inc. Combo Pure Solutions light blue label NG Inc. Red Crown High Test Lye red label Boyer Corporation Boyer Potassium Hydroxide Flakes white label Boyer Corporation 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.


February 19, 2020 Contigo Reannounces Recall of 5.7 Million Kids Water Bottles Due to Choking Hazard; Additional Incidents with Replacement Lids Provided in Previous Recall

This recall involves Contigo Kids Cleanable water bottles and replacement lids that were given to consumers as part of the August 2019 recall of this product. The base and cover of the clear silicone spout will always be BLACK. Only black colored spout base and spout cover models are included in this recall. Contigo is printed on the rim and along the front near the bottom of the bottle. The water bottles come in three sizes (13 ounce, 14 ounce and 20 ounce) and four colors (solid color, graphics, stainless steel and stainless steel solid colors). The water bottles were sold individually as well as in two-packs and three-packs. Read more.


February 6, 2020 Sun Organic Recalls Wintergreen Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning

This recall includes all 2-, 4-, 8-, and 16-fluid-ounce amber glass bottles of Sun Essential Oils, Wintergreen sold prior to April 12, 2019. The label on each bottle displays the Sun Essential Oils logo, an image of an American Wintergreen plant, states "Wintergreen," and lists the size of the container. Read more.


September 10, 2019 Healing Solutions Recalls Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements; Risk of Poisoning

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.


September 4, 2019 Artizen Oils Recalls Essential Oils Due to Failure to Meet Child Resistant Packaging Requirements, Risk of Poisoning

This recall includes all 1- and 2-ounce clear glass bottles of wintergreen and birch essential oils purchased prior to April 15, 2019. The label on each bottle displays Artizen Oils' logo and the name of the product. Read more.