RecallRadar

FDA Drug recall D-0042-2021

Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharmaceutical Co., Ltd., Shanghai, 200245, China…

On 2020-10-28 the FDA classified a Class III recall of Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharmaceutical Co., Ltd., Shanghai, 200245, China… by Evenus Pharmaceutical Laboratories, citing DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0042-2021
ClassificationClass III
Statusterminated
Initiated2020-10-06
Published2020-10-28
Last updated2026-09-13 11:52 UTC
CompanyEvenus Pharmaceutical Laboratories
DistributionCO

Product

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

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

Identifiers

ndc0781-6172-22
ndc0781-6172-86
code_infoLot #: 20011831, Exp. Date 12/2021; 20041431, Exp. Date 03/2022

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0042-2021%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.