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Drug recalls

Drug recalls from FDA, newest first.
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2 recalls

Rhino Choco VIP 10X Chocolate

Rhino Choco VIP 10X Chocolate contains undeclared Tadalafil, which may lower blood pressure to dangerous levels.

FDA

Teva Metoprolol Succinate Extended-Release Tablets

Metoprolol Succinate Extended-Release Tablets failed dissolution specifications.

Moderate risk, FDA, Drug dissolving problem

3 recalls

Lockout Supplements Boner Bears Chocolate Syrup

Boner Bears Chocolate Syrup contains undeclared sildenafil, which may lower blood pressure to dangerous levels.

FDA

Agebox iKids-Growth Day and Night Formula Capsules

Agebox iKids-Growth (Day Formula) capsules contain undeclared ibutamoren.

Moderate risk, FDA, Hidden drug ingredient

Wizcure Pharmaa Eye Drops and Fluorescein Sodium Ophthalmic Strips

Vista Tears, Vista Gel, Vista Meibo Tears, Vista Gonio, CHNaO, Bio Glo, and BioGlo eye products lack assurance of sterility.

Moderate risk, FDA, Sterility problem

3 recalls

Slate Run Eptifibatide Injection

Eptifibatide Injection's carton labeling states 75 mg/100 mL vial for weight-adjusted bolus dosing, but the approved statement is for weight-adjusted infusion.

Low risk, FDA, Labeling error

AvKARE Amantadine HCl Capsules

Amantadine HCl capsules failed dissolution specifications.

Moderate risk, FDA, Drug dissolving problem

Adbry (Tralokinumab-Ldrm) Injection

Adbry injection may not be sterile due to wool fiber particulate matter in one unit.

Moderate risk, FDA, Sterility problem

4 recalls

Shaman Botanicals White Vein Advanced Alkaloids Chewable Tablets

White Vein Advanced Alkaloids Chewable Tablets contain more 7-Hydroxymitragynine than labeled, which could cause adverse health effects.

High risk, FDA, Labeling error

Green Lumber Dietary Supplement

Green Lumber Dietary Supplement may contain undeclared tadalafil, a prescription drug, which can cause life-threatening side effects.

FDA

New York Blood Center Apheresis Platelets, Leukocytes Reduced

Apheresis Platelets, Leukocytes Reduced did not meet platelet yield specifications.

Moderate risk, FDA, Quality testing problem

Community Blood Center Of Greater Kansas City Apheresis Red Blood Cells

Apheresis Red Blood Cells, Leukocytes Reduced were distributed after a donor's health history screening was not adequately performed.

Low risk, FDA, Blood donor screening

1 recall

Fresenius Kabi Acyclovir, Ketamine, Thiamine and Vancomycin Injections

Acyclovir sodium, ketamine HCl, thiamine HCl, and vancomycin HCl injections lack assurance of sterility.

Moderate risk, FDA, Sterility problem

4 recalls

Asteria Health Estradiol and Testosterone Sterile Pellets

Estradiol and testosterone sterile pellets may contain metal particulate matter.

Moderate risk, FDA, Foreign object

Unichem Doxazosin Tablets

Doxazosin Tablets, USP, 4 mg are imprinted with the wrong ID.

Low risk, FDA, Labeling error

Meitheal Pharmaceuticals Cetrorelix Acetate for Injection (Kit)

Cetrorelix Acetate for Injection kits may have missing or duplicated needles.

Moderate risk, FDA, Device defect

American Red Cross Apheresis Platelets and Red Blood Cells

American Red Cross Apheresis Platelets and Red Blood Cells, for which Babesia testing was not performed, were distributed.

Moderate risk, FDA, Quality testing problem

3 recalls

Accord BioPharma Udenyca Prefilled Syringe

Udenyca injection was stored at room temperature instead of refrigerated.

High risk, FDA, Processing problem

American Health Packaging Oxycodone Hydrochloride Tablets

Oxycodone Hydrochloride Tablets have defective card seals, which can cause tablets to come out of their cavities.

Moderate risk, FDA, Packaging defect

American National Red Cross Red Blood Cells, Leukocytes Reduced, Irradiated

American National Red Cross - Johnstown, PA products, for which Babesia testing was not performed, were distributed.

Moderate risk, FDA, Quality testing problem

1 recall

Pro Numb Tattoo Numbing Spray

Pro Numb Tattoo Numbing Spray is recalling its Pro Numb Tattoo Numbing Spray because of cGMP deviations.

Moderate risk, FDA, Manufacturing problem

1 recall

American National Red Cross Red Blood Cells

American National Red Cross Red Blood Cells, for which Babesia testing was not performed, were distributed.

Moderate risk, FDA, Quality testing problem

5 recalls

Taro Diclofenac Sodium Topical Gel 3%

Diclofenac Sodium Topical Gel 3% has a viscosity that is slightly lower than the limit.

Moderate risk, FDA, Quality testing problem

Granules Trazodone Hydrochloride Tablets

Trazodone Hydrochloride tablets contain foreign tablets or capsules.

Moderate risk, FDA, Foreign object

Stratford Care: 36 products

Keto-C Antiseptic Wipes labeled as medicated contain a non-medicated otic flush due to a product mix-up.

Moderate risk, FDA, Labeling error

Green Lumber Natural Fuel For Men Capsules

Green Lumber Natural Fuel For Men capsule contains tadalafil without approval.

High risk, FDA, Hidden drug ingredient

Handelnine Global Rheumacare Capsules

Rheumacare capsules contain lead.

High risk, FDA, Manufacturing problem

2 recalls

Unichem Bisoprolol Fumarate and Hydrochlorothiazide Tablets

Bisoprolol Fumarate and Hydrochlorothiazide tablets fail to meet impurity specification limits.

Moderate risk, FDA, Drug impurity

Central Valley Medicated Cattle Feed Supplements

Cattle feed formulations contain incorrect levels of thiamine and selenium, posing potential selenium toxicity.

High risk, FDA, Wrong nutrient levels

3 recalls

Akkarco Ashfiat Alharamain Energy Support

Ashfiat Alharamain Energy Support contains undeclared tadalafil, which may pose health risks.

High risk, FDA, Hidden drug ingredient

Greenstone Methylprednisolone Tablets Dosepak

Methylprednisolone tablets have incorrect dosing information on the blister foil.

Moderate risk, FDA, Labeling error

Novadoz Glycopyrrolate Oral Solution

Glycopyrrolate Oral Solution failed impurities and degradation specifications.

Low risk, FDA, Drug impurity

1 recall

Sato INON ACE Antacid Tablets

Failed Disintegration Specifications: above the time expected.

Moderate risk, FDA, Quality testing problem

1 recall

Haleon Parodontax Active Gum Health Mouthwash

Parodontax mouthwash may have missing or illegible lot and expiration date coding on the bottles.

Low risk, FDA, Labeling error

2 recalls

Baxter Sterile Water for Irrigation

Sterile Water for Irrigation contains plastic particles from the bottle rim that can float into the solution.

Moderate risk, FDA, Foreign object

Qunol Extra Strength Turmeric Capsules

Qunol Extra Strength Turmeric Capsules may contain mold contamination.

Moderate risk, FDA, Contamination

1 recall

Zydus Pharmaceuticals Icosapent Ethyl Capsules

Icosapent Ethyl capsules may be subpotent due to oxidation from leakage of capsule contents.

Moderate risk, FDA, Wrong drug strength

2 recalls

Rising Pharmaceuticals Furosemide Tablets

Furosemide Tablets contain a foreign substance.

Moderate risk, FDA, Foreign object

Specialty Process Labs Thyroid USP

Thyroid, USP is subpotent.

Moderate risk, FDA, Wrong drug strength

1 recall

Cipla Diclofenac Sodium Topical Gel 1%

Diclofenac Sodium Topical Gel, 1% failed pH specifications.

Low risk, FDA, Quality testing problem

1 recall

Cipla USA Lanreotide Injection

Lanreotide Injection contains particulate matter.

Moderate risk, FDA, Foreign object

5 recalls

Encon Safety Products Aquarion Preserved Cartridges

The Aquarion Preserved Cartridges have cGMP deviations.

Moderate risk, FDA, Manufacturing problem

Advanced Pharmaceutical Technology TESTO-100 CIII Testosterone Pellets

Testo-100 Ciii (testosterone 100 mg) pellets may lack assurance of sterility due to potential microbial contamination.

Moderate risk, FDA, Sterility problem

Sun Pharmaceutical Clindamycin Phosphate Topical Solution

Failed Impurities/Degradation: Out of Specification results for Total Impurities and for Assay.

Low risk, FDA, Drug impurity

Alvogen Levothyroxine Sodium Tablets Thy-Tabs

Levothyroxine Sodium Tablets, USP, Thyro-Tabs may contain 88 mcg tablets instead of 150 mcg tablets.

Moderate risk, FDA, Labeling error

Gold Star Distribution Advil, Aleve, Tylenol and More Over-the-Counter Medicines

Gold Star Distribution medicines have CGMP deviations.

Moderate risk, FDA, Manufacturing problem

1 recall

Taro Pharmaceuticals Fluocinolone Acetonide Topical Solution

Fluocinolone Acetonide Solution Topical Solution failed impurity specifications due to an out-of-specification result for known impurity D.

Low risk, FDA, Drug impurity

1 recall

Herbs Forever Ayurvedic Herbal Supplements

HerbsForever Hingwastik Churna and Gastro Care dietary supplements may contain undeclared wheat, posing a risk of serious allergic reactions.

High risk, FDA, Undeclared wheat

3 recalls

123Herbals Silintan 25 Pills

Silintan capsules contain undeclared meloxicam, which can cause serious life-threatening events.

High risk, FDA, Hidden drug ingredient

SpecGx Oxycodone and Acetaminophen CII Tablets

Oxycodone and Acetaminophen CII Tablets may have a missing imprint on the tablets.

Moderate risk, FDA, Quality testing problem