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Drug recall · FDA · Published October 6, 2020

eVenus Pharmaceutical Laboratories recalls Desflurane, USP Liquid for Inhalation, 240 mL, Rx Only, Manufactured by: Shanghai Hengrui Pharmaceutical Co., Ltd.,

eVenus Pharmaceutical Laboratories recalls Desflurane 240mL inhalation liquid due to leaking container risk. This prescription drug may cause injury if used improperly. Contact for return instructions.

🇺🇸 FDA recall #D-0042-2021DrugeVenus Pharmaceutical Laboratories ›
Take action

Contact the company & request your remedy

Recalling firmeVenus Pharmaceutical Laboratories506 Carnegie Ctr, Suite 100 · Princeton, NJ 08540-6243
No email on file for this recall — reach the company by phone or its official page instead.No email on file — write to the address above instead.
✎ GovInfoNow plain-language explainer

What happened, in plain English

eVenus Pharmaceutical Laboratories is recalling Desflurane liquid for inhalation because the container may leak. This could lead to improper medication delivery or accidental exposure if the product leaks. Read more at govinfonow.com/recall/36734-evenus-desflurane-liquid-recall-leaking-container-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/36734-evenus-desflurane-liquid-recall-leaking-container-hazard · Updated October 4, 2026 · FDA enforcement record: FDA #D-0042-2021

Cite this page

“eVenus Desflurane Liquid Recall: Leaking Container Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36734-evenus-desflurane-liquid-recall-leaking-container-hazard. Based on FDA recall #D-0042-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0042-2021%22&limit=1).

Why it’s dangerous

The container may leak, which could cause improper medication delivery or accidental exposure to the user. Leaking could lead to incorrect dosing or potential injury if the liquid comes into contact with skin or eyes.

Who’s affected

Prescription drug users who have the specific Desflurane 240mL liquid with the described lot numbers and expiration dates are affected. Patients using this medication for anesthesia are most at risk.

How to tell if you have this one

Check for the product name 'Desflurane, USP Liquid for Inhalation, 240 mL', Rx Only, manufactured by Shanghai Hengrui Pharmaceutical Co., Ltd. Look for lot numbers 20011831 (expiring 12/2021) or 20041431 (expiring 03/2022).

  • Brand
    eVenus Pharmaceutical Laboratories
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the lot number and expiration date on the container to confirm if it's in the recalled range.

  2. Contact Your Provider

    Reach out to your healthcare provider for guidance on whether to stop using the medication or need a replacement.

✎ GovInfoNow

Questions people ask

Is this product safe to use?

The product may leak, which could cause improper medication delivery or accidental exposure. Do not use if you have the recalled lot numbers.

How do I know if I have the recalled product?

Check for lot numbers 20011831 (expiring 12/2021) or 20041431 (expiring 03/2022) on the container.

What should I do if I have the recalled product?

Contact your healthcare provider for guidance on whether to stop using the medication or need a replacement.

Take action

Contact eVenus Pharmaceutical Laboratories

We’ve drafted a message you can send eVenus Pharmaceutical Laboratories to request your refund or repair — edit it as you like.

Subject: Recall D-0042-2021 — eVenus Pharmaceutical Laboratories eVenus Pharmaceutical Laboratories

Hello,

I own a eVenus Pharmaceutical Laboratories that is covered by recall D-0042-2021 from eVenus Pharmaceutical Laboratories.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #D-0042-2021 (October 6, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0042-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA