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

530 recalls, newest first

Class II · Moderate risk

Dr. Reddy's Quetiapine Fumarate Tablets

Failed USP Dissolution Test Requirements: During analysis of long term stability studies at 3 months time point, an OOS was reported for Quetiapine Fumarate Tablets, 25 mg.

Terminated Dissolution failure Dr. Reddy's Laboratories, Inc. NDC 55111-249-05 D-059-2013
Class II · Moderate risk

Lactated Ringer's Injection USP

Chemical Contamination: The IV solutions were packaged in AVIVA containers which may contain trace levels of cumene hydroperoxide (CHP).

Terminated Chemical / undeclared Baxter Healthcare Corp. NDC 0338-6307-02 D-1690-2012
Class II · Moderate risk

0.9% Sodium Chloride Injection USP

Chemical Contamination: The IV solutions were packaged in AVIVA containers which may contain trace levels of cumene hydroperoxide (CHP).

Terminated Chemical / undeclared Baxter Healthcare Corp. NDC 0338-6304-02 D-1689-2012

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