Sun Pharmaceutical Industries, Inc. recalls Vecuronium Bromide for Injection 10 mg*, *1mg/mL when reconstituted to 10 mL Lyophilized, 10 x 10 mg vials, Rx only,
Sun Pharmaceutical recalls Vecuronium Bromide injection vials due to glass particles detected. This could cause serious injury if injected. Affected vials have specific NDC numbers and expiration dates. Contact Sun Pharmaceutical for details.
Use caution until it’s fixed
Presence of Particulate Matter: Foreign matter identified as glass detected in Vecuronium Bromide for Injection.
Contact the company & request your remedy
What happened, in plain English
Sun Pharmaceutical is recalling Vecuronium Bromide injection vials because glass particles were found inside. This could cause serious injury if the medication is injected. The recall affects specific vial and carton numbers with expiration dates up to March 2019. Read more at govinfonow.com/recall/39254-sun-pharmaceutical-vecuronium-bromide-injection-recall-foreign-glass-particles-found.
Source Summary by GovInfoNow · govinfonow.com/recall/39254-sun-pharmaceutical-vecuronium-bromide-injection-recall-foreign-glass-particles-found · Updated October 5, 2026 · FDA enforcement record: FDA #D-0372-2019
Cite this page
“Sun Pharmaceutical Vecuronium Bromide Injection Recall: Foreign Glass Particles Found.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/39254-sun-pharmaceutical-vecuronium-bromide-injection-recall-foreign-glass-particles-found. Based on FDA recall #D-0372-2019 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0372-2019%22&limit=1).
Why it’s dangerous
Glass particles in the injection vial could cause serious injury when injected into a person's body. This is a foreign material that may lead to tissue damage or other complications during medical procedures.
Who’s affected
Healthcare professionals who use this medication for anesthesia. Patients receiving this drug under medical supervision are at risk if the vial is used without proper checks.
How to tell if you have this one
Check for vial numbers NDC 47335-931-40 or 47335-931-44. The vials were manufactured with lot numbers JKS0443A, JKS0444A, or JKS0477A and expire by March 2019.
- Brand
Sun Pharmaceutical- Category
Drug
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
- Classification
Class I- Status
Terminated- Distribution
Nationwide in the USA- NDC
47335-931-40, 47335-931-44, 47335-932-40, 47335-932-44
| Recall number | Product, codes & lots | Quantity |
|---|---|---|
| D-0372-2019 | Vecuronium Bromide for Injection 10 mg*, *1mg/mL when reconstituted to 10 mL Lyophilized, 10 x 10 mg vials, Rx only, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway Halol-389 350, Gujarat, India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 NDC 47335-931-40 [vial] NDC 47335-931-44 [carton]; Lot #: JKS0443A, JKS0444A, JKS0477A, EXP 03/2019 | 12,534 cartons, 125,340 vials |
| D-0373-2019 | Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to 20 mL Lyophilized, 10 x 20 mg vials, Rx Only, Manufactured by: Sun Pharmaceutical Industries Ltd. Halol-Baroda Highway Halol-389 350, Gujarat, India. Distributed by: Sun Pharmaceutical Industries, Inc. Cranbury, NJ 08512 NDC: 47335-932-40 [vial] 47335-932-44 [carton]; Lot #: JKS0400A, EXP 03/2019 | 1,384 cartons, 13,840 vials |
What to do — step by step
Check Vial Numbers
Look for NDC numbers 47335-931-40 or 47335-931-44 on the vial or carton.
Contact Manufacturer
Reach out to Sun Pharmaceutical Industries, Inc. at Cranbury, NJ 08512 for further assistance.
Questions people ask
Is this product safe to use?
No, the presence of glass particles makes this product unsafe for injection. Do not use the vials with lot numbers JKS0443A, JKS0444A, or JKS0477A.
What should I do if I have the recalled vials?
Contact Sun Pharmaceutical Industries, Inc. at Cranbury, NJ 08512 to get instructions on what to do with the vials.
When was this product recalled?
The recall was issued for vials manufactured with lot numbers JKS0443A, JKS0444A, or JKS0477A that expire by March 2019.
Contact Sun Pharmaceutical
We’ve drafted a message you can send Sun Pharmaceutical to request your refund or repair — edit it as you like.
Subject: Recall D-0372-2019 — Sun Pharmaceutical Sun Pharmaceutical Hello, I own a Sun Pharmaceutical that is covered by recall D-0372-2019 from Sun Pharmaceutical. 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-0372-2019 (January 3, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0372-2019 to see it in context.
- Plain-language summary written by qwen3:4b on October 5, 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.