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LowClass IIITerminated

FDA Drug recall · Reported October 28, 2020

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

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

Recall #
D-0042-2021
Affected scope
9210 units
Initiated
October 6, 2020
Compiled from official public sources by the editorial team.
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eVenus Pharmaceutical Laboratories recalled Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengru… - a low-severity action.

Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengru… was recalled by eVenus Pharmaceutical Laboratories in October 28, 2020. Reason: DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking.. Check the official notice for the remedy. Verify recall #D-0042-2021 with the FDA Drug before acting.

The recall

eVenus Pharmaceutical Laboratories issued this low-severity FDA Drug recall-DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking..

Low
severity level
9K units
affected scope
Class III
classification
October 28, 2020
reported

Sourced from official FDA Drug enforcement records. Verify recall #D-0042-2021 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Drug action (record #D-0042-2021) was formally reported on October 28, 2020, with the manufacturer initiating the action on October 6, 2020. It is classified under Low severity (Class III), with a current status of Terminated. eVenus Pharmaceutical Laboratories is listed as the recalling firm, operating out of Princeton, NJ. Federal records list the affected scope as 9210 units.

The documented reason for this recall is: DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking. Distribution data in the federal record shows the product reached: CO only. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

Within the same product category the archive holds 6 closely related recalls, 5 from FDA Drug - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.

Drugs & Medications recalls over time

Where this recall sits in its category - 14,287 drugs & medications recalls on record

-50005001,0001,5002,000 2006201220152018202120242026 263
Severity2487872426High severity (most serious)Moderate severityLow severity
Where this recall sits in the database

Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Low

Affected scope

9210 units

Related Recalls

6

5 from same agency

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.

Recall Profile

Structured summary of the FDA Drug recall record
Attribute Value
Agency U.S. Food and Drug Administration
Severity class Low (Class III)
Status Terminated
Recall number D-0042-2021
Date reported October 28, 2020
Date initiated October 6, 2020
Recalling firm eVenus Pharmaceutical Laboratories
Firm location Princeton, NJ
Affected scope 9210 units
Distribution CO only

Profile values are sourced directly from the official FDA Drug enforcement record. Source: U.S. Food and Drug Administration.

Scale of Impact

9210 units units affected - limited or regional distribution scale.

Regional (<10K units) ✓ This recall
Multi-state (10K – 100K units) -
Large-scale (100K – 1M units) -
Massive (≥1M units) -

Bracket cutoffs follow federal recall-disclosure conventions; bar widths scale linearly within each bracket. Source: PlainRecalls analysis of U.S. Food and Drug Administration filings.

What to do with this recall

Match your product against the recall record, then act on the agency remedy.

  • Check the recall number (D-0042-2021) and product description against the item you own. Search the archive
  • Confirm the current status with FDA Drug before acting, recall details can be updated.
  • Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next

This page summarizes the official FDA Drug record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.

Frequently Asked Questions

What product was recalled?
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. Recalled by eVenus Pharmaceutical Laboratories. Units affected: 9210 units.
Why was this product recalled?
DEFECTIVE CONTAINER: Desflurane Liquid for Inhalation 240 mL may be leaking.
Which agency issued this recall?
This recall was issued by the FDA Drug on October 28, 2020. Severity: Low. Recall number: D-0042-2021.
Where was the recalled product distributed?
Distribution: CO only.
How do I check if my product is affected by a recall?
Check the product description and recall number (D-0042-2021) against your product. Visit the official FDA Drug website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device?
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.

Nearby Recalls in This Category

Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Drug, reported October 28, 2020. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.