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

Reason for Recall
CGMP Deviations: Presence of NDMA impurity detected in product.
Initiated
12-02-2019
Reported
12-18-2019
Quantity
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
Preferred Pharmaceuticals, Inc
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