Recalls: Personal Care

This recall involves bottles of Geri-Care Brand over-the-counter acetaminophen and aspirin. The acetaminophen is 500mg with 1,000 tablets in the bottle. The aspirin was sold in 81mg with 300 and 1,000 tablets in the bottle and 325mg with 250 and 1,000 tablets in the bottle. Product Count Extra Strength Acetaminophen 500mg Tablets 1,000 Regular Strength Enteric Coated Aspirin 325mg Tablets 250 Regular Strength Enteric Coated Aspirin 325mg Tablets 1,000 Adult Low Dose Enteric Coated Aspirin 81mg Tablets 300 Adult Low Dose Enteric Coated Aspirin 81mg Tablets 1,000 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 all models of the Massimo Percussion Massage Gun. The massage guns have 20 speed levels and came with six massage heads and a built-in rechargeable lithium ion battery. They were sold in black, silver, gold, and blue, all were model number EM003. Model numbers can be found on the Product information card in the package. Read more.

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.

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.

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.

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 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 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 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.