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

98 recalls · Class I, newest first

Class I · High risk

Walgreens

Microbial contamination of non-sterile products.

Terminated Microbial contamination Vi-Jon, LLC NDC 0363-7162-38 D-1510-2022
Class I · High risk

Walgreens

Microbial contamination of non-sterile products.

Terminated Microbial contamination Vi-Jon, LLC NDC 0363-8166-38 D-1509-2022
Class I · High risk

Swan

Microbial contamination of non-sterile products.

Terminated Microbial contamination Vi-Jon, LLC NDC 0869-0166-38 D-1507-2022
Class I · High risk

Rexall

Microbial contamination of non-sterile products.

Terminated Microbial contamination Vi-Jon, LLC NDC 55910-183-38 D-1506-2022
Class I · High risk

meijer

Microbial contamination of non-sterile products.

Terminated Microbial contamination Vi-Jon, LLC NDC 41250-708-38 D-1504-2022
Class I · High risk

Kroger

Microbial contamination of non-sterile products.

Terminated Microbial contamination Vi-Jon, LLC NDC 30142-899-38 D-1503-2022
Class I · High risk

Insulin Glargine

Labeling: Missing label: Label missing from some prefilled pens.

Terminated Labeling / mix-up Mylan Pharmaceuticals Inc NDC 49502-394-71 D-1292-2022
Class I · High risk

Launch Sequence Aphrodisia Capsules

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Loud Muscle Science D-1338-2022
Class I · High risk

Launch Sequence Euphoria Capsules

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Loud Muscle Science D-1337-2022
Class I · High risk

Launch Sequence Capsules

Marketed Without An Approved NDA/ANDA: Product found to contain undeclared tadalafil, an ingredient found in FDA approved products for the treatment of male sexual enhancement, making this an unapproved drug.

Terminated Chemical / undeclared Loud Muscle Science D-1336-2022
Class I · High risk

Morphine Sulfate extended-Release Tablets

Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.

Terminated Labeling / mix-up Bryant Ranch Prepack, Inc. NDC 63629-1089-01 D-1188-2022
Class I · High risk

Morphine Sulfate extended-Release Tablets

Labeling: Label Mix-up: bottles labeled as Morphine Sulfate 60 mg Extended-Release tablets contain Morphine Sulfate 30 mg Extended-Release tablets and bottles labeled as Morphine Sulfate 30 mg Extended-Release tablets may contain Morphine Sulfate 60 mg Extended-Release tablets.

Terminated Labeling / mix-up Bryant Ranch Prepack, Inc. D-1187-2022

Recalls by year