Mylan Institutional LLC recalls Daptomycin for Injection, 500 mg/vial, Single-Dose Vial, Rx only, Sterile, Manufactured for: Mylan Institutional, LLC,
Mylan recalls Daptomycin 500mg vials due to possible particulate matter. This could cause serious injury if injected. Affected vials have specific lot numbers and expiration dates.
Use caution until it’s fixed
Presence of Particulate Matter
Contact the company & request your remedy
What happened, in plain English
Mylan is recalling Daptomycin for Injection vials that may contain particulate matter. This could cause serious injury if injected into the body. The recall affects specific vials with lot number 7605112 and expiration date 10/2021. Read more at govinfonow.com/recall/36952-mylan-daptomycin-injection-recall-particulate-matter-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/36952-mylan-daptomycin-injection-recall-particulate-matter-hazard · Updated October 5, 2026 · FDA enforcement record: FDA #D-1484-2020
Cite this page
“Mylan Daptomycin Injection Recall: Particulate Matter Hazard.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36952-mylan-daptomycin-injection-recall-particulate-matter-hazard. Based on FDA recall #D-1484-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1484-2020%22&limit=1).
Why it’s dangerous
Particulate matter in the injection vials could enter the bloodstream during administration, potentially causing serious injury or death. This risk is higher when the vial is used for injection without proper filtration.
Who’s affected
Healthcare professionals who use Daptomycin for Injection vials with lot number 7605112 and expiration date 10/2021 are affected. Patients receiving this medication under a prescription are at risk if the recalled vials are used.
How to tell if you have this one
Check for lot number 7605112 on the vial label with expiration date 10/2021. The product is a 500 mg/vial single-dose injection for prescription use only.
- Brand
Mylan- Category
Drug
What to do — step by step
Check Vial Label
Look for lot number 7605112 and expiration date 10/2021 on the vial label.
Questions people ask
Is this product safe to use?
The recall indicates a potential risk of particulate matter that could cause serious injury if injected. Do not use the recalled vials.
What should I do if I have the recalled vial?
The recall record does not specify a remedy, so contact Mylan Institutional LLC for guidance.
How can I verify if my vial is recalled?
Check for lot number 7605112 and expiration date 10/2021 on the vial label.
Contact Mylan
We’ve drafted a message you can send Mylan to request your refund or repair — edit it as you like.
Subject: Recall D-1484-2020 — Mylan Mylan Hello, I own a Mylan that is covered by recall D-1484-2020 from Mylan. 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-1484-2020 (July 7, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1484-2020 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.