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

13 recalls · Class II, newest first

Class II · Moderate risk

Repaskin 30

cGMP Deviations; product does not comply with cGMP requirements

Ongoing cGMP deviation Sesderma, SL NDC 63181-0010-1 D-0849-2016
Class II · Moderate risk

Repaskin 50

cGMP Deviations; product does not comply with cGMP requirements

Ongoing cGMP deviation Sesderma, SL NDC 63181-0011-1 D-0848-2016
Class II · Moderate risk

Repaskin 30

cGMP Deviations; product does not comply with cGMP requirements

Ongoing cGMP deviation Sesderma, SL NDC 63181-0012-1 D-0845-2016
Class II · Moderate risk

Repaskin 50

cGMP Deviations; product does not comply with cGMP requirements

Ongoing cGMP deviation Sesderma, SL NDC 63181-0013-1 D-0844-2016
Class II · Moderate risk

1% Lidocaine HCl Injection

Presence of Particulate Matter: particulate matter identified as iron oxide, was found embedded in the neck of glass vials.

Ongoing Particulate / foreign matter Hospira, Inc. NDC 0409-4279-02 D-1815-2015

Recalls by year