Recall Radar

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

Recall 19-194 · August 29, 2019 · Sandoz

What to doConsumers should immediately secure the medications to keep them out of the sight and reach of children and contact Sandoz for a free replacement child resistant bottle cap. Once the medication is secured, consumers can continue to use the medication as directed.

Read the official CPSC notice

Recall at a glance

Recall number
19-194 (CPSC)
Recall date
August 29, 2019
Brand
Sandoz
Category
Candles and household goods
Products
Losartan Potassium and Ezetimibe prescription drug bottles
Hazard
Failure to Meet Child-Resistant Closure Requirements
Hazard type
Choking and ingestionPoisoning and toxic substances
Remedy
Replace
Units
About 636,000
Made in
Slovenia
Last updated by CPSC
August 29, 2019

What was recalled

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

Is my product affected?

Compare your product with the details below, including model numbers where listed.

  • Losartan Potassium and Ezetimibe prescription drug bottles · About 636,000 units

Photos from the recall notice

Where it was sold

Companies named in the notice: 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.; Sandoz Inc., of Princeton, N.J..

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 history and context

Sandoz appears in 3 CPSC recalls on record. See all Sandoz recalls.

Since 2019 CPSC has recorded 166 recalls in the candles and household goods category, 33 recalls of them in the past 12 months.

Frequently asked questions

What was recalled?

Losartan Potassium and Ezetimibe prescription drug bottles (About 636,000 units). This recall involves bottles of prescription medications Losartan Potassium and Ezetimibe from Sandoz with certain lot numbers.

Why was it recalled?

CPSC lists the reason as: Failure to Meet Child-Resistant Closure Requirements.

What should I do if I own one?

Consumers should immediately secure the medications to keep them out of the sight and reach of children and contact Sandoz for a free replacement child resistant bottle cap. Once the medication is secured, consumers can continue to use the medication as directed.

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Source: U.S. Consumer Product Safety Commission recall data, shown as published and last updated by CPSC on August 29, 2019. Details can change; the official notice is the authority. If your product may be recalled, stop and read the notice before deciding what to do. Terms and disclaimer.