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Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharma...

FDA Recall #D-0042-2021 — Class III — October 6, 2020

Recall #D-0042-2021 Date: October 6, 2020 Classification: Class III Status: Terminated

Product Description

Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharmaceutical Co., Ltd., Shanghai, 200245, China for Sandoz Inc. Princeton, NJ 08540, NDC 0781-6172-22

Reason for Recall

DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking.

Recalling Firm

eVenus Pharmaceutical Laboratories — Princeton, NJ

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

9210 units

Distribution

CO only

Code Information

Lot #: 20011831, Exp. Date 12/2021; 20041431, Exp. Date 03/2022

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated

What Should You Do?

Stop using this medication immediately and contact your pharmacist or doctor. Do not flush medications down the drain. Return the product to the place of purchase for a refund or replacement.

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