US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 30, 2018 (8 years ago)

Lidocaine Patch 5% (700 mg) ,(NDC 0591-3525-11), 30 envelopes containing 1 patch each/ 30…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Stability Specifications

What was recalled

Lidocaine Patch 5% (700 mg) ,(NDC 0591-3525-11), 30 envelopes containing 1 patch each/ 30 Patches/Carton (NDC 0591-3525-30)

Recalling firm
Teva Pharmaceuticals USA
NDC code
0591-3525-11
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0857-2018

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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