Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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FDA Drug Recalls

1,563 recalls, newest first

Class II · Moderate risk

Phenobarbital Oral Solution

Labeling: Incorrect or Missing Lot and/or Exp Date - the label contains an incorrect Exp Date.

Terminated Labeling / mix-up Lohxa LLC NDC 70166-536-02 D-1131-2019
Class II · Moderate risk

Fayosim (levonorgestrel and ethinyl estradiol)

Failed Impurities/Degradation Specifications: Out-of-specification results observed in related substance test (Any Other Individual Impurity and Total impurities) in Ethinyl Estradiol Tablets USP 0.01mg at 12 month long term stability study.

Terminated Impurity / degradation Lupin Pharmaceuticals Inc. NDC 68180-860-11 D-1057-2019
Class II · Moderate risk

Gavilyte-N

Labeling Not Elsewhere Classified; orange and cherry flavor packets incorrect list "natural lemon flavor" as an ingredient

Terminated Labeling / mix-up Lupin Somerset NDC 43386-050-19 D-1113-2019
Class III · Low risk

Diclofenac Sodium Topical Solution

Defective Container: firm discovered samples stored horizontally as well as product quality complaints from customers for bottles leaking.

Terminated Packaging defect Ingenus Pharmaceuticals Llc NDC 50742-308-05 D-1058-2019
Class III · Low risk

Clindamycin Injection

Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point

Terminated Impurity / degradation Pfizer Inc. NDC 47781-621-94 D-1072-2019
Class III · Low risk

Clindamycin Injection

Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point

Terminated Impurity / degradation Pfizer Inc. NDC 47781-620-94 D-1071-2019
Class III · Low risk

Clindamycin Injection

Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point

Terminated Impurity / degradation Pfizer Inc. NDC 47781-619-94 D-1070-2019
Class III · Low risk

Cleocin Phosphate

Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point

Terminated Impurity / degradation Pfizer Inc. NDC 0009-3447-01 D-1069-2019
Class III · Low risk

Cleocin Phosphate

Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point

Terminated Impurity / degradation Pfizer Inc. NDC 0009-3124-01 D-1068-2019
Class III · Low risk

Cleocin Phosphate

Failed Impurities/Degradation Specifications: High out-of-specification (OOS) results were demonstrated for several specified impurities at the 24-month time point

Terminated Impurity / degradation Pfizer Inc. NDC 0009-6582-02 D-1067-2019
Class I · High risk

Blue Fusion Capsules

Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared ingredients: Sildenafil, Tadalafil, desmethyl carbodenafil, dithiodesmethyl carbodenafil, scutellarin, and daidzein.

Terminated Chemical / undeclared Ata International Inc D-1085-2019
Class II · Moderate risk

Losartan 50mg Tablet

CGMP Deviations; Detection of trace amounts of an unexpected impurity found in an active pharmaceutical ingredient (API) - N-Methylnitrosobutyric acid (NMBA).

Terminated Nitrosamine impurity RemedyRepack Inc. D-1081-2019

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