US Drug Recall Register
Class III · Low risk Terminated Initiated Jun 9, 2021 (5 years ago)

Phytonadione Tablets 5 mg, Rx Only, 30 Tablets (3x10) Unit Dose, Manufactured for: AvKARE…

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

Why it was recalled

Failed Impurities Specification: Out of specification when measuring the impurity degradant D level.

What was recalled

Phytonadione Tablets 5 mg, Rx Only, 30 Tablets (3x10) Unit Dose, Manufactured for: AvKARE Pulaski, TN 38478. NDC 50268-661-13

Recalling firm
AVKARE Inc.
NDC code
50268-661-13
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0631-2021

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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