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Drug recalls

Drug recalls from FDA, newest first.
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7 recalls

Baxter Cefazolin in Dextrose Injection

Cefazolin in Dextrose Injection may contain particulate matter, which can cause pulmonary emboli, blood vessel occlusions, and phlebitis.

High risk, FDA, Foreign object

American Regent Nitroglycerin, Cyanocobalamin, Aminocaproic Acid, Atropine Sulfate, Acetylcysteine, Selenious Acid, Multrys, Papaverine HCl, Tralement and Nicardipine Injections

American Regent injections contain particulate matter.

High risk, FDA, Contamination

Micro Labs Dorzolamide HCl and Timolol Maleate Ophthalmic Solution

Dorzolamide HCl and Timolol Maleate Ophthalmic Solution has defective container caps that may break.

Moderate risk, FDA, Packaging defect

Proin ER, Phenylpropanolamine Hydrochloride Extended-Release Tablets

Proin ER tablets failed dissolution specifications, which can affect drug release.

Moderate risk, FDA, Drug dissolving problem

Ascend Laboratories Dabigatran Etexilate Capsules

Dabigatran Etexilate Capsules failed impurity and degradation specifications.

Low risk, FDA, Drug impurity

Mylan Mycophenolate Mofetil for Injection

Mycophenolate Mofetil for Injection USP contains a precipitate.

Moderate risk, FDA, Quality problem

3 recalls

Fresenius Kabi Glycopyrrolate, Lidocaine and Naropin Injections

Fresenius Kabi Glycopyrrolate, Lidocaine and Naropin Injections contain particulate matter.

Moderate risk, FDA, Foreign object

Rohto Cooling Eye Drops

Rohto Cooling Eye Drops lack assurance of sterility.

Moderate risk, FDA, Sterility problem

Precision Dose Glycopyrrolate Oral Solution

Glycopyrrolate Oral Solution failed impurities and degradation specifications due to an unidentified impurity.

Moderate risk, FDA, Drug impurity

1 recall

Rising Pharma Cetirizine Hydrochloride Tablets

Cetirizine Hydrochloride Tablets may be contaminated with ranitidine, which could cause serious reactions.

High risk, FDA, Contamination

6 recalls

Rising Cyproheptadine Hydrochloride Syrup

Cyproheptadine Hydrochloride Syrup has crystallized and particles floating in the bottle.

Moderate risk, FDA, Foreign object

Major Pharmaceuticals Levothyroxine Sodium Tablets

Levothyroxine Sodium Tablets are subpotent.

Moderate risk, FDA, Wrong drug strength

Ascend Laboratories Amlodipine and Olmesartan Medoxomil Tablets

Amlodipine and Olmesartan Medoxomil Tablets failed dissolution specifications, with Olmesartan Medoxomil content below specifications.

Moderate risk, FDA, Drug dissolving problem

Trokendi XR, Topiramate Extended-Release Capsules

Trokendi XR, topiramate extended-release capsules failed dissolution specifications.

Low risk, FDA, Drug dissolving problem

Ascend Laboratories Dabigatran Etexilate Capsules

Dabigatran etexilate capsules failed impurity and degradation specifications during stability testing.

Low risk, FDA, Drug impurity

Bionpharma Divalproex Sodium Delayed-Release Tablets

Divalproex Sodium Delayed-Release Tablets may contain foreign tablets or capsules.

Moderate risk, FDA, Foreign object

1 recall

BD ChloraPrep Clear

BD ChloraPrep Clear may have an open or incomplete seal on the applicator packaging.

Moderate risk, FDA, Sterility problem

2 recalls

Chiesi Cleviprex Clevidipine Injectable Emulsion

Cleviprex injectable emulsion lacks assurance of sterility.

Moderate risk, FDA, Sterility problem

Bell Pharmaceuticals Carbamide Peroxide Ear Drops

SubPotent Drug: low pH and significantly reduced assay (~0.6% vs expected ~6 7%).

Moderate risk, FDA, Wrong drug strength

2 recalls

Padagis Nystatin Cream

Nystatin Cream USP is subpotent, with low assay results from stability testing.

Moderate risk, FDA, Wrong drug strength

Sun Pharmaceutical Fexofenadine Hydrochloride Tablets

Fexofenadine Hydrochloride Tablets failed impurities and degradation specifications.

Low risk, FDA, Drug impurity

2 recalls

Somerset Therapeutics Pemetrexed, Bortezomib and Azacitidine for Injection

Pemetrexed, Bortezomib, and Azacitidine for Injection lack sterility assurance.

Moderate risk, FDA, Manufacturing problem

Gasco and Drogueria San Juan Isopropyl Alcohol

Isopropyl alcohol 70% is subpotent.

Moderate risk, FDA, Wrong drug strength

3 recalls

QuVa Pharma Methohexital Sodium

Methohexital Sodium failed impurities and degradation specifications.

Moderate risk, FDA, Drug impurity

Medline Remedy Specialized Silicone Cream (Hydraguard-D)

Medline Remedy Specialized Silicone Cream has formaldehyde levels exceeding specification.

Moderate risk, FDA, Quality testing problem

Avet Methohexital Sodium for Injection

Methohexital Sodium for Injection failed impurities and degradation specifications.

Moderate risk, FDA, Drug impurity

3 recalls

Cipla Cinacalcet Hydrochloride Tablets

CGMP Deviations: presence of N-nitroso-cinacalcet, above the acceptable daily intake (ADI).

Moderate risk, FDA, Drug impurity

Lannett Dextroamphetamine and Amphetamine Extended-Release Capsules

These capsules are labeled as extended-release but contain only immediate-release pellets.

Moderate risk, FDA, Labeling error

Enovachem Pharmaceuticals Lidocaine HCl Injection

Accucaine kits containing Lidocaine HCl Injection lack assurance of sterility.

Moderate risk, FDA, Sterility problem

2 recalls

Lupin Pharmaceuticals Glucagon Emergency Kit for Low Blood Sugar

CGMP deviation: OOS result observed for the Gliding Force functionality test during 12-month long term stability testing.

Moderate risk, FDA, Quality testing problem

Hikma Gemcitabine Injection

Gemcitabine Injection was stored incorrectly.

Moderate risk, FDA, Processing problem

2 recalls

Accord Healthcare Levothyroxine Sodium Tablets

Levothyroxine Sodium Tablets are subpotent.

Moderate risk, FDA, Wrong drug strength

Lupin Prednisolone Acetate Ophthalmic Suspension

The ophthalmic suspension contains a foreign substance.

Moderate risk, FDA, Foreign object

2 recalls

CareFusion 213 BD ChloraPrep and PurPrep Applicators

BD ChloraPrep and PurPrep applicators may be unsterile or contaminated with fungus, potentially causing serious infection or death.

Moderate risk, FDA, Sterility problem

Accord BioPharma Imuldosa Injection

Imuldosa injection lacks assurance of sterility.

Moderate risk, FDA, Sterility problem

1 recall

TNVitamins Organic Moringa Capsules and Powder

TNVitamins 100% Organic Moringa Capsules and Powder are contaminated with Salmonella, which can cause serious infections.

High risk, FDA, Salmonella

1 recall

Povi-One, 10% Povidone-Iodine Oral Antiseptic

Povi-One, 10% Povidone-Iodine Oral Antiseptic has sub potency.

Moderate risk, FDA, Wrong drug strength

4 recalls

Sun Pharmaceutical Perampanel CIII Tablets

Perampanel CIII Tablets, 6mg, may contain a 10mg tablet due to a label mix-up.

Moderate risk, FDA, Labeling error

Camber Lacosamide Tablets

Lacosamide Tablets may contain a foreign tablet, Selexipag 1000 mcg.

Moderate risk, FDA, Foreign object

ANI Pharmaceuticals Hydroxyzine Hydrochloride Oral Solution

HydrOXYzine Hydrochloride Oral Solution contains a foreign substance.

Low risk, FDA, Foreign object

Abbott Determine HIV 1/2 Ag/Ab Combo

Abbott Diagnostics has noticed a negative trend in false positive complaints for Determine" HIV 1/2 Ag/Ab Combo 25T kits (Catalog 7D2648).

Moderate risk, FDA

2 recalls

Direct Rx Duloxetine and Cymbalta Capsules

Duloxetine D/R contains an impurity above the FDA recommended interim limit.

Moderate risk, FDA, Drug impurity

Amgen Corlanor and Sensipar Tablets

Corlanor (ivabradine) tablets contain a foreign substance, and Sensipar (cinacalcet) Tablets have CGMP deviations.

Moderate risk, FDA, Foreign object

2 recalls

Major Methylergonovine Maleate Tablets

Methylergonovine Maleate Tablets are subpotent.

Moderate risk, FDA, Wrong drug strength

Ajanta Pharma Fenofibrate Capsules

Fenofibrate Capsules, USP 200 mg, have CGMP deviations.

Moderate risk, FDA, Manufacturing problem

1 recall

Keystone Topical Anesthetic Gels

Topical anesthetic gels may have defective containers with incomplete seals.

Moderate risk, FDA, Packaging defect

1 recall

Endo Buprenorphine HCl Injection

Buprenorphine HCl injection has crystallization identified as Buprenorphine free base.

Moderate risk, FDA, Quality problem

1 recall

Ajanta Pharma Aripiprazole Tablets

Aripiprazole Tablets USP are mislabeled, containing Voriconazole Tablets instead.

Moderate risk, FDA, Labeling error

6 recalls

Dabur Antifungal, Antibiotic and Hydrocortisone Creams and Ointments

Dabur Antifungal, Antibiotic and Hydrocortisone Creams and Ointments have CGMP deviations.

Moderate risk, FDA, Manufacturing problem

Inventia Healthcare Chlorthalidone Tablets

Chlorthalidone Tablets fail dissolution specifications.

Moderate risk, FDA, Drug dissolving problem