June 24, 2026DrugsFDA
Dabur India Limited recalls Med Pride, Bacitracin Zinc Ointment, 500 units, 1oz (28.3g) tubes, Manufactured for: Shield Line LLC, 59 Hook Road, Bayo
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Dabur India Limited recalls Med Pride, Bacitracin Zinc Ointment, 500 units, 0.9g packets Net Wt 130g, 144 count box, Manufactured for: Shield Line L
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Dabur India Limited recalls Cura Hongos, Crema Antifungica, Clotrimazole 1%, 2oz (57g) tubes, Dist by/por: Pharmadel LLC, New Castle, DE 19720, Made
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Dabur India Limited recalls Rapidol, Triple Antibiotic First Aid Ointment, Bacitracin Zinc 400 units, Neomycin Sulfate 3.5 mg, Polymyxin-B Sulfate 5
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Dabur India Limited recalls Lil Drug Store, Triple Antibiotic Ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Dabur India Limited recalls Circle K, triple antibiotic ointment, Bacitracin Zinc (400 units), Neomycin Sulfate (3.5 mg), Polymyxin-B Sulfate (5000
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Dabur India Limited recalls Lucky Super Soft, First Aid Triple Antibiotic Ointment, Bacitracin zinc 400 units, neomycin sulphate 3.5 mg, polymyxin B
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Dabur India Limited recalls Lucky Super Soft, Antifungal Athlete's Foot Cream, Clotrimazole 1% Cream, Net Wt. 1.5 oz (42.5g) Tubes, Manufactured for
Hazard: CGMP Deviations; deficiencies observed during FDA inspection
June 24, 2026DrugsFDA
Inventia Healthcare Limited recalls Chlorthalidone Tablets, USP, 25 mg, [100 or 1000] Tablets pr bottle, Rx only, Manufactured by: Inventia Healthcare Limit
Hazard: Failed Dissolution Specifications
June 24, 2026DrugsFDA
Sandoz Inc recalls Focalin XR (dexmethylphenidate HCl) 5 mg, 30 extended-release capsules per bottle, Rx only, Manufactured by Societal CDM
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
June 24, 2026DrugsFDA
Keystone Industries recalls safco SensiCaine-Ultra (20% Benzocaine), Topical Anesthetic Gel, Strawberry Flavor, 1 oz. (29.6mL), Distributed by: Sa
Hazard: Defective container:may contain bottles with incomplete seals
June 24, 2026DrugsFDA
Keystone Industries recalls PureLife, TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, 1 oz (30mL), Strawberry Flavor, Manufactured for Pure Life, LLC, Man
Hazard: Defective container:may contain bottles with incomplete seals
June 24, 2026DrugsFDA
Keystone Industries recalls Dental City TOPICAL ANESTHETIC GEL, BENZOCAINE 20%, Strawberry Flavor, 1 OZ (30 g), Distributed by Dental City, 3205 Ye
Hazard: Defective container:may contain bottles with incomplete seals
June 24, 2026DrugsFDA
Keystone Industries recalls Burkhart topical anesthetic gel, benzocaine 20 %, Strawberry Flavor, 1 oz (30 mL), Manufactured for Burkhart Dental Supp
Hazard: Defective container:may contain bottles with incomplete seals
June 24, 2026DrugsFDA
Keystone Industries recalls DHP Topical Anesthetic Gel, Benzocaine 20%, Strawberry Flavor, 1 oz. (30 g), Manufactured for and Distributed by Dental
Hazard: Defective container:may contain bottles with incomplete seals
June 24, 2026DrugsFDA
Keystone Industries recalls Quala Dental Products, Topical Anesthetic Gel, 20 % Benzocaine, Strawberry Flavor Net Contents: 1 oz (30 g), Quala Denta
Hazard: Defective container:may contain bottles with incomplete seals
June 24, 2026DrugsFDA
Keystone Industries recalls Pearson Quality Topical Anesthetic Gel (20% Benzocaine), Mint Flavor, Net Contents: 1 oz (3o g), Manufactured for: Pears
Hazard: Defective container:may contain bottles with incomplete seals
June 24, 2026DrugsFDA
Par Health USA, LLC recalls Buprenorphine HCl, CIII, Injection, 0.3 mg/mL, 5 x 1 mL Single Dose Vials per Carton, Rx Only, For Intramuscular or Intr
Hazard: Crystallization; identified as Buprenorphine free base
June 24, 2026DrugsFDA
Ajanta Pharma USA Inc recalls Aripiprazole Tablets USP, Rx only, 30 mg, 30 tablets, Marketed by: Ajanta Pharma USA Inc., Bridgewater, NJ 08807, Made i
Hazard: Product Mix-Up: A bottle containing Voriconazole Tablets 50 mg was labelled and distributed as Aripiprazole Tablets USP 30 mg.
June 24, 2026DrugsFDA
IntegraDose Compounding Services LLC recalls Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride, syringe, IntegraDose Compounding Services, LLC. 3650 Victoria St N, Su
Hazard: Subpotent Drug
June 24, 2026DrugsFDA
PAI Holdings LLC recalls VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 52 Grams Sorbitol in
Hazard: Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
June 24, 2026DrugsFDA
PAI Holdings LLC recalls VistaPharm, KERR INSTA-CHAR IN AN SORBITOL BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 26 Grams Sorbitol in
Hazard: Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
June 24, 2026DrugsFDA
PAI Holdings LLC recalls VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 50 Grams Activated Charcoal in 240 ml (8 fl oz), dist
Hazard: Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
June 24, 2026DrugsFDA
PAI Holdings LLC recalls VistaPharm, KERR INSTA-CHAR IN AN AQUEOUS BASE WITH CHERRY FLAVOR, 25 Grams Activated Charcoal in 120 ml (4 fl oz), dist
Hazard: Does Not Meet USP or OTC Monograph: Product did not meet the Over-the-Counter (OTC) Monograph M023
June 24, 2026DrugsFDA
Glenmark Pharmaceuticals Inc., USA recalls Alyacen 7/7/7, Norethindrone and Ethinyl Estradiol Tablets USP, 0.5mg/0.035mg, 0.75mg/0.035mg, 1 mg/0.0.35mg, 3 Blister
Hazard: Failed Impurities/Degradation Specifications: This recall is being initiated due to out-of-specification results total impurities.
June 17, 2026DrugsFDA
BEEKEEPER'S NATURALS USA INC. recalls BEEKEEPER'S NATURALS Saline Nasal Spray, Sinus Congestion Rinse, Made with Propolis + Xylitol, 1 FL OZ (30 mL) per bottl
Hazard: Microbial Contamination of Non-Sterile Products
June 17, 2026DrugsFDA
SUN PHARMACEUTICAL INDUSTRIES INC recalls Budesonide Inhalation Suspension, 1mg/2mL, 30 x 2 mL Sterile Single-Dose Ampules (5 Single-Dose Ampules per pouch, 6 pou
Hazard: Presence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution
June 17, 2026DrugsFDA
Ascend Laboratories, LLC recalls Minocycline Hydrochloride Extended-Release Tablets, USP, 115 mg, 30-count bottle, Rx Only, Manufactured by: Alkem Labora
Hazard: Failed Dissolution Specifications: An out-of-specification (OOS) result was observed during the 9th month of dissolution test analysis
June 17, 2026DrugsFDA
Haleon US Holdings LLC recalls Gas-X Extra Strength, SIMETHICONE 125 mg/ANTIGAS, packaged in a) 120 SoftGels (UPC 3 00674 35041 9, b) 72 SoftGels (UPC
Hazard: Chemical Contamination: contamination with a diluted propylene glycol-based coolant from a machine leakage during the packaging process.
June 17, 2026DrugsFDA
Golden State Medical Supply Inc. recalls GSMS Incorporated, NIACIN EXTENDED-RELEASE TABLETS, USP, 1,000 MG, 90 tablets, Rx only, Manufactured by Kremers Urban Ph
Hazard: Failed Dissolution Specifications: During 12-month long-term stability testing, subject lot was out of specification (low) for stage 3 dissolution at the 24-hour timepoint.