Recalls: Containers and Packaging
This recall involves sodium hydroxide drain cleaner sold in a 2-pound white plastic bottle with a continuous thread closure cap. Alliance Chemical, Sodium Hydroxide Flakes, Pure Lye, Caustic Soda, NaOH, and Drain Cleaner are printed on the blue and white label. The second recalled product involves sodium hydroxide sold in a 5-pound clear bag with a white and black label that states Sodium Hydroxide Flake and Caustic Soda Flake. Read more.
This recall involves Modernist Pantry Kitchen Alchemy bags of sodium hydroxide. The product was sold in 50 grams and 400 grams black and orange resealable bags and marketed for food preparation use. The Modernist Pantry logo and a female cook appear on the front of the bag. Kitchen Alchemy, Sodium Hydroxide, pH Buffering and the product weight are printed on the label. Read more.
This recall involves GEO Wintergreen Organic Essential Oil and GEO Alleviate Organic Essential Oil Blend in amber glass bottles with black caps. The Wintergreen oil was sold in a 5 mL bottle and the Alleviate oil in a 15 mL bottle. The bottle's label displays the GEO logo, product name and the volume amount of the bottle. SKU 990181 can be found on the label above and to the left of the bar code of the Wintergreen essential oil and SKU 990305 on the label above and to the left of the bar code of the Alleviate essential oil. Read more.
This recall involves Epicure Prep Bowls (Set of Four). Epicure and the product code "1004242" are printed on the outside bottom of the box. The clear glass bowls have plastic purple lids. Epicure is stamped on the bowls and the lids, and each bowl is marked with the following measurements: "50 ml," "125ml," "175ml," "1/4 cup," "1/2 cup," and "3/4 cup." Read more.
This recall involves dōTERRA Deep Blue, PastTense and Deep Blue Touch Essential Oils in 10 mL glass bottles with rollerball applicator and black cap. The product name, volume amount, SKU, and dōTERRA logo are printed on the product labels. The following lot number can be found on the bottom of the bottle: Name Size Lot Number SKU Deep Blue 10 ml 183055, 183232, 190882, 191362, 191484, 192563, 192694, 200853, 202203, 202412, 201622, 202262 60200144 PastTense 10 ml 182621, 190072, 190452, 190512, 190573, 190642, 190662, 190702, 190801, 190921, 191232, 191404, 193451, 200242, 200422, 200932, 201292, 201351, 201392, 201401, 201471, 201481, 201493, 201541, 201551, 201571, 201603, 201673, 201744, 201754, 201822, 201971, 202043 31350001 Deep Blue Touch 10 ml 183094, 190802, 192314, 192666, 193222, 201141, 201923 60200145 Read more.
This recall involves bottles of the prescription drug Evrysdi, a prescription medicine used to treat spinal muscular atrophy (SMA) in adults and children 2 months of age and older. The recalled 100 mL amber bottles have "Evrysdi (risdiplam) for oral solution," the dosage and "NDC 20242-175-07" on the front of the bottle labels. Read more.
This recall involves 1/2 fl. oz (15 mL) amber glass bottles with black caps of deSensua Wintergreen Essential Oil, Birch Essential Oil and Pain Soother Essential Oil. The black, gold and blue labels on each bottle displays the deSensua logo, product name and the volume amount of the bottle. The Wintergreen Essential Oil has UPC code 760921403266, the Birch Essential Oil has UPC code 760921403129 and the Pain Soother Essential Oil has UPC code 760921403051 printed on the back of the label. Read more.
This recall involves blister packages of prescription medications. The name and strength of the medication, "For Institutional Use only," "Rx Only," lot number and expiration date are printed on the outside of the package as well as on the individual blister units. The Dr. Reddy's logo and NDC number are printed on the outside of the package. The recalled medications include the following: Recalled Prescription Drugs NDC Numbers Carton Configurations Lot Numbers Expiration Dates Imatinib Mesylate Tablets 100 mg 43598-344-31 3 blister cards of 10 tablets H2000138 2022-0630 Imatinib Mesylate Tablets 400 mg 43598-345-31 3 blister cards of 10 tablets H2000127 2022-0630 Pregabalin Capsules 50 mg 43598-292-66 5 blister cards of 10 capsules T900876 2021-0630 Pregabalin Capsules 75 mg 43598-293-66 5 blister cards of 10 capsules T901021 2021-0731 Pregabalin Capsules 100 mg 43598-294-66 5 blister cards of 10 capsules T901022 2021-0731 Pregabalin Capsules 150 mg 43598-295-66 5 blister cards of 10 capsules T901023 2021-0731 Sevelamer Carbonate Tablets 800 mg 55111-789-11 4 blister cards of 25 tablets T801003, T000009, T900221 2020-1031, 2021-1231, 2021-0228 Tadalafil Tablets 5 mg 43598-575-31 3 blister cards of 10 tablets T000376 2022-0131 Tadalafil Tablets 20 mg 43598-573-31 3 blister cards of 10 tablets T000425 2022-0228 Read more.
This recall involves Scalpa Numb Maxium Strength Topical Anesthestic Cream in a 10 gram black and white tube with a white cap. "SCALPANUMB" and "Maximum Strength Topical Anesthetic Cream" are printed on the label. The expiration date is marked as EXP 202307 on the crimped end of the tube. Batch number 1000000101, Code: C1 and the UPC code 857076008689 are printed on the outside of the box. Read more.
This recall involves 50, 80, 100, 125, 200, 250 and 300-count bottles of Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets. The bottles are plastic with a child-resistant closure. For a full list of the recalled products, visit www.excedrin.com/products/discontinued. Read more.