Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA drug recalls in 2018

Every FDA drug recall initiated in 2018, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,681 recalls, newest first.

Class II · Moderate risk

Fluconazole Injection

Labeling: Label mix-up - A complaint was received of one bag of Fluconazole Injection, Iso-Osmotic Sodium Chloride Diluent, USP, 2mg/mL, 50 mL found within the package of 100 mL bags.

Terminated Labeling / mix-up Renaissance Lakewood, LLC NDC 36000-002-10 D-0696-2018
Class II · Moderate risk

Labetalol Hydrochloride Injection

Defective Container: Cracked glass at the rim surface of glass vials, covered by the stopper and crimp seal.

Terminated Packaging defect Hospira Inc. A Pfizer Company NDC 0409-2267-20 D-0576-2018
Class II · Moderate risk

Vardenafil HCl

cGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life Kalchem International, Inc. NDC 60592-330-05 D-0582-2018
Class II · Moderate risk

0.9% Sodium Chloride Irrigation USP

Presence of Particulate Matter: Customer complaint of particulate matter which has been identified as polyethylene, which is consistent with the material used to manufacture the container cap was received.

Terminated Particulate / foreign matter B. Braun Medical Inc NDC 0264-2201-00 D-0549-2018
Class II · Moderate risk

PVP Scrub Solution

Subpotent Drug: product not meeting the iodine assay level requirements through the labeled expiry.

Terminated Wrong potency / content Medline Industries Inc NDC 53329-938-04 D-0546-2018
Class I · High risk

Bella Capsules

Marketed Without An Approved NDA/ANDA: This product contains undeclared sibutramine. The presence of sibutramine, a previously approved controlled substance that was withdrawn from the U.S. market in October 2010 due to safety concerns, in this tainted product renders it an unapproved drug for which safety and efficacy have not been established and therefore subject to recall.

Terminated Chemical / undeclared Bella All Natural D-0593-2018
Class II · Moderate risk

SyrSpend SF Suspending Base

Microbial contamination of Non-Sterile Product; product contamination with yeast and mold (Paecilomyces saturatus and Aspergillus fumigatus).

Terminated Microbial contamination Fagron, Inc NDC 51552-1079-5 D-0547-2018
Class II · Moderate risk

Valacyclovir Tablets USP 1 gram

Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).

Terminated Temperature excursion Hetero Labs Limited Unit V NDC 31722-705-30 D-0602-2018
Class II · Moderate risk

Valganciclovir Tablets

Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir Tablets USP 1 gram were exposed to higher temperature at airport or cargo and in the same consignment of Famciclovir complaint batch (D-0415-2018).

Terminated Temperature excursion Hetero Labs Limited Unit V NDC 31722-832-60 D-0601-2018
Class II · Moderate risk

Acyclovir Tablets

Presence of Foreign Tablet/Capsule; cartons labeled to contain Acyclovir tablets may contain Torsemide tablets in some of the blister cavities.

Terminated Particulate / foreign matter Apace KY LLC NDC 50268-061-11 D-0544-2018
Class II · Moderate risk

Fluticasone propionate USP

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8276-3 D-0539-2018
Class II · Moderate risk

Cyanocobalamin USP

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8044-1 D-0538-2018
Class II · Moderate risk

Methylcobalamin

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8142-1 D-0537-2018
Class II · Moderate risk

Biotin USP

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8142-1 D-0536-2018
Class II · Moderate risk

Ascorbic Acid USP

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8120-6 D-0535-2018
Class II · Moderate risk

Verapamil HCl USP for prescription compounding

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8039-6 D-0534-2018
Class II · Moderate risk

Vardenafil HCl USP

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8575-2 D-0533-2018
Class II · Moderate risk

Ursodiol USP for prescription compounding

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8038-6 D-0531-2018
Class II · Moderate risk

Tretinoin USP for prescription compounding

CGMP Deviations: Lack of stability data and controls to support the manufacturers assigned retest or expiration date in firm's container/closure system.

Terminated Stability / shelf life American Pharmaceutical Ingredients LLC NDC 58597-8033-2 D-0530-2018

Recalls by year