Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

FDA drug recalls in 2019

Every FDA drug recall initiated in 2019, newest first, with its risk class, status and the reason the FDA recorded. Use the cause and risk filters to narrow the year down.

1,788 recalls, newest first.

Class II · Moderate risk

Clobazam Oral Suspension

Microbial Contamination of Non-Sterile Products: Out-of-specification results for Microbial Enumeration Tests USP <61> was observed.

Terminated Microbial contamination Bionpharma Inc. NDC 69452-116-45 D-1519-2019
Class II · Moderate risk

Temozolomide Capsules

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Terminated Cross-contamination Deva Holding AS - Cerkezkoy Subesi NDC 67877-542-07 D-1513-2019
Class II · Moderate risk

Temozolomide Capsules

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Terminated Cross-contamination Deva Holding AS - Cerkezkoy Subesi NDC 67877-541-07 D-1512-2019
Class II · Moderate risk

Temozolomide Capsules

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Terminated Cross-contamination Deva Holding AS - Cerkezkoy Subesi NDC 67877-540-07 D-1511-2019
Class II · Moderate risk

Temozolomide Capsules

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Terminated Cross-contamination Deva Holding AS - Cerkezkoy Subesi NDC 67877-539-07 D-1510-2019
Class II · Moderate risk

Temozolomide Capsules

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Terminated Cross-contamination Deva Holding AS - Cerkezkoy Subesi NDC 67877-538-07 D-1509-2019
Class II · Moderate risk

Temozolomide Capsules

CGMP Deviations: product was manufactured that did not prevent possible cross contamination with beta lactam products.

Terminated Cross-contamination Deva Holding AS - Cerkezkoy Subesi NDC 67877-537-07 D-1508-2019
Class II · Moderate risk

LA FRESH travel lite Sunnyside Lotion Wipe silky

Marketed without an Approved NDA/ANDA: The product may be construed a sunscreen due to labeling of the product and comments about the product found on e-commerce websites.

Terminated Unapproved drug La Fresh Group, Inc. D-1566-2019
Class II · Moderate risk

Fungo Off Capsules

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Terminated cGMP deviation Herbal Doctor Remedies D-1629-2019
Class II · Moderate risk

Asma Stopper Capsules

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Terminated cGMP deviation Herbal Doctor Remedies D-1628-2019
Class II · Moderate risk

Anemia Off

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Terminated cGMP deviation Herbal Doctor Remedies D-1627-2019
Class II · Moderate risk

Appetrol Capsules

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Terminated cGMP deviation Herbal Doctor Remedies D-1626-2019
Class II · Moderate risk

Mental Tonic Capsules

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Terminated cGMP deviation Herbal Doctor Remedies D-1625-2019
Class II · Moderate risk

Thyro-Lo

CGMP Deviations: Products were manufactured outside of the controls required by current Good Manufacturing Practices.

Terminated cGMP deviation Herbal Doctor Remedies D-1624-2019

Recalls by year