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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 86568

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
October 06, 2020
Product types
Drug
Classifications
Class III
Statuses
Terminated
Recalling firm wording
eVenus Pharmaceutical Laboratories

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

1 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 1

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

D-0042-2021
Recall number
D-0042-2021
Initiated
October 06, 2020
Classification
Class III
Status
Terminated
Quantity
9210 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

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

Distribution pattern

CO only