US Drug Recall Register

FDA Drug Recalls

11,815 recalls · Class II, newest first

Class II · Moderate risk Terminated

Timolol-Latanoprost P-F

Reason Subpotent Drug

ImprimisRx NJ D-1578-2019
Class II · Moderate risk Terminated

Clobazam Oral Suspension

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

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

Temozolomide Capsules

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

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

Temozolomide Capsules

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

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

Temozolomide Capsules

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

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

Temozolomide Capsules

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

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

Temozolomide Capsules

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

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

Temozolomide Capsules

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

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

CVS Health Children's Allergy Relief Liquid Medication…

Reason CGMP Deviations: Recall as a precautionary measure due to potential risk of product contamination with the bacteria B. cepacia.

Unipharma, Llc. NDC 69842-261-01 D-1631-2019
Class II · Moderate risk Terminated

LA FRESH travel lite Sunnyside Lotion Wipe silky

Reason 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.

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

Fungo Off Capsules

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

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

Asma Stopper Capsules

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

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

Anemia Off

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

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

Appetrol Capsules

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

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

Mental Tonic Capsules

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

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

Thyro-Lo

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

Herbal Doctor Remedies D-1624-2019
Class II · Moderate risk Terminated

Smoke End Capsules

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

Herbal Doctor Remedies D-1623-2019
Class II · Moderate risk Terminated

Detensin

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

Herbal Doctor Remedies D-1622-2019
Class II · Moderate risk Terminated

Yeast Douche Powder

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

Herbal Doctor Remedies D-1621-2019
Class II · Moderate risk Terminated

Worm Off

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

Herbal Doctor Remedies D-1620-2019
Class II · Moderate risk Terminated

Vertigo Off Capsules

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

Herbal Doctor Remedies D-1619-2019
Class II · Moderate risk Terminated

Thyro-H

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

Herbal Doctor Remedies D-1618-2019