November 2016 FDA Recall Levoxyl by Pfizer Inc.
D-0150-2017 - Superpotent
This Class II drug recall was voluntarily initiated by Pfizer Inc. on November 7, 2016 for the product Levoxyl. The FDA reported the reason for recall as superpotent. The product was distributed Nationwide and the recall is currently terminated.
Recall Number: D-0150-2017
Superpotent
11-07-2016
11-30-2016
2,666 bottles
Recall Profile & Regulatory Data
Class II - is a situation in which use of, or exposure to, a violative product may cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote
Enforcement Status About Enforcement Status
Current regulatory stage of the recall event.
Current regulatory stage of the recall event.
Terminated
Recalling Firm About Recalling Firm
The firm responsible for the recall.
The firm responsible for the recall.
Pfizer Inc.
Voluntary / Mandated About Voluntary / Mandated
Indicates if the firm acted on its own or under FDA order.
Indicates if the firm acted on its own or under FDA order.
Voluntary: Firm initiated
Drugs
Initial Notification About Initial Notification
Method by which the firm first notified the public.
Method by which the firm first notified the public.
Letter
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
Nationwide
05-01-2020
Product Description About Product Description
Full technical description of the product.
Full technical description of the product.
LEVOXYL(R) (levothyroxine sodium tablets, USP), 200 mcg, 100 count bottles, Rx only, Manufactured and Distributed by: King Pharmaceuticals, Inc., Bristol, TN 37620, NDC 60793-860-01
Batch or Lot Expiration Information
Lot# 16H21, Exp. 08/2017
