December 2019 FDA Recall Drug by Preferred Pharmaceuticals, Inc
D-0617-2020 - CGMP Deviations
This Class II drug recall was voluntarily initiated by Preferred Pharmaceuticals, Inc on December 2, 2019 for the product Drug. The FDA reported the reason for recall as cgmp deviations. The product was distributed in CA, FL and the recall is currently terminated.
Recall Number: D-0617-2020
CGMP Deviations: Presence of NDMA impurity detected in product.
12-02-2019
12-18-2019
316 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.
Preferred Pharmaceuticals, 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.
E-Mail
Distribution Pattern About Distribution Pattern
General area of initial distribution.
General area of initial distribution.
CA, FL
05-09-2023
Product Description About Product Description
Full technical description of the product.
Full technical description of the product.
Ranitidine Tablets, USP 150 mg, OTC, a.) 30 count bottle (NDC 68788-7078-03), b.) 60 count bottle (NDC 68788-7078-06), Mfg: Amneal Pharmaceuticals
Batch or Lot Expiration Information
Lot# : I2519H, Exp. 12/20; I2719O, Exp. 12/20; J1419O, Exp. 12/20; J2819L, Exp. 12/20