Independent register of U.S. FDA drug recalls · updated Oct 14, 2026
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FDA Drug Recalls

14,806 recalls, newest first

Class III · Low risk

Auryxia (ferric citrate)

Presence of Foreign Substance: Reports have been received of damaged StripPax packets containing silica gel desiccant potentially allowing the silica gel granules to make contact with Auryxia tablets in the bottle.

Terminated Particulate / foreign matter Keryx Biopharmaceuticals, Inc. NDC 59922-631-01 D-0133-2018
Class II · Moderate risk

Neutrogena Elevated 4-Holiday Trays

Defective Container: products showed leakage (bubbles, foaming) of propellant and product from the container valve cup area.

Terminated Packaging defect Johnson & Johnson D-0245-2018
Class III · Low risk

Enoxaparin Sodium

Labeling: Label Error on Declared Strength. A single syringe labeled as 150 mg/1.0 mL was found packaged in a blister labeled as 120 mg/mL

Terminated Labeling / mix-up Sanofi-Aventis U.S. LLC NDC 0955-1012-10 D-0153-2018
Class II · Moderate risk

Gabapentin Tablets

Labeling: Label Mix-Up.some bottles labeled as Gabapentin 800 mg contain Gabapentin 600 mg

Terminated Labeling / mix-up Solco Healtcare US LLC NDC 43547-0333-50 D-0155-2018
Class II · Moderate risk

Viokace (pancrelipase)

Subpotent Drug: One lot of Viokace is being recalled since product stability testing results did not meet the specifications for enzyme profile.

Terminated Wrong potency / content Allergan NDC 58914-117-10 D-0154-2018
Class III · Low risk

Bull Capsules

Marketed without an Approved NDA/ANDA; product found to be tainted with sildenafil

Terminated Chemical / undeclared BYL Solutions Inc. D-0414-2018

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