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

Allergy Relief

Failed Impurities/Degradation Specifications

Terminated Impurity / degradation Aurolife Pharma, LLC NDC 49035-995-62 D-1869-2019
Class II · Moderate risk

Allergy Relief

Failed Impurities/Degradation Specifications

Terminated Impurity / degradation Aurolife Pharma, LLC NDC 46122-387-23 D-1866-2019
Class II · Moderate risk

Allergy Relief

Failed Impurities/Degradation Specifications

Terminated Impurity / degradation Aurolife Pharma, LLC NDC 60000-409-53 D-1865-2019
Class II · Moderate risk

RELPAX (eletriptan HBr)

Microbial Contamination of Non-Sterile Products: contamination with Burkholderia and Pseudomonas.

Terminated Microbial contamination Pfizer Inc. NDC 0049-2340-45 D-1845-2019

Recalls by year