Sandoz Recalls Losartan Potassium and Ezetimibe Prescription Drug Bottles Due to Failure to Meet Child-Resistant Closure Requirements

Losartan Potassium and Ezetimibe prescription drug bottles

Date of Recall
2019-08-29

CPSC Release Number
19-194

Manufactured In
Slovenia

Units
About 636,000

Distributor
Sandoz Inc., of Princeton, N.J.

Sold By
Clinics and pharmacies nationwide as a prescribed medicine from July 2018 through August 2019. The container was included in the price of the medication, which varied based on quantities prescribed, health insurance terms and other factors.

Problem/Hazard
The prescription drug packaging is not child resistant as required by the Poison Prevention Packaging Act, posing a poisoning risk if swallowed by children.

Injuries/Incidents
None Reported

Description

This recall involves bottles of prescription medications Losartan Potassium and Ezetimibe from Sandoz with certain lot numbers. The recalled bottles have "Sandoz," the name of the medication, dosage, and NDC on the front of the bottle labels and the lot number and expiration date on the side of the bottle labels. The recall includes the following:

Recalled Prescription Drugs

NDC Numbers

Lot Numbers

Expiration Date

Ezetimibe 10mg Tablets

0781-5690-31

JE4491

Aug-2020

30 count bottle

JE4492

Aug-2020

JE4493

Aug-2020

JE4495

Aug-2020

JG0308

Sep-2020

JG0310

Sep-2020

JG0311

Sep-2020

JG0312

Sep-2020

JG5061

Sep-2020

JG5063

Sep-2020

JK8921

Oct-2020

JK8922

Oct-2020

JK8923

Oct-2020

JK8924

Oct-2020

JL5535

Oct-2020

JM2253

Oct-2020

JM2254

Oct-2020

JM2255

Oct-2020

JM2257

Oct-2020

JM2258

Oct-2020

JM2259

Oct-2020

JM5986

Oct-2020

JM5987

Oct-2020

Ezetimibe 10mg Tablets

0781-5690-92

JE4481

Aug-2020

90 count bottle

JG0249

Sep-2020

JK8989

Oct-2020

JN0764

Jan-2021

Losartan Potassium 50mg Tablets

0781-5701-31

HV9471

Feb-2020

30 count bottle

Remedy
Replace

Consumer Contact
Sandoz at 800-525-8747 from 8:30 a.m. to 5 p.m. ET Monday to Friday or online at www.us.sandoz.com and click on "Patients and Customers" then "Product Safety Notices."

Recall Comments

No comments have been posted.
Be the first to add a comment!