Edge Pharma, LLC recalls Ceftazidime Sterile Ophthalmic Solution for Injection Preservative Free 11.25mg / 0.5ml (22.5mg/ml) 0.5ml per syringe.
Edge Pharma recalls Ceftazidime Sterile Ophthalmic Solution for Injection due to expired sterility testing media. This compounded drug may not be sterile, risking eye infections. Contact customer service for details.
Lower-risk recall
Lack of Assurance of Sterility; the media used to conduct post-compounding sterility testing for the Methotrexate product was expired.
Contact the company & request your remedy
What happened, in plain English
Edge Pharma is recalling Ceftazidime Sterile Ophthalmic Solution for Injection because the sterility testing media used was expired. This could mean the solution isn't sterile, potentially causing eye infections if used. Read more at govinfonow.com/recall/37294-edge-pharma-ceftazidime-ophthalmic-solution-recall-sterility-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/37294-edge-pharma-ceftazidime-ophthalmic-solution-recall-sterility-risk · Updated October 5, 2026 · FDA enforcement record: FDA #D-0238-2021
Cite this page
“Edge Pharma Ceftazidime Ophthalmic Solution Recall: Sterility Risk.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/37294-edge-pharma-ceftazidime-ophthalmic-solution-recall-sterility-risk. Based on FDA recall #D-0238-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0238-2021%22&limit=1).
Why it’s dangerous
The sterility testing media used to check if the solution is clean expired. If the solution isn't sterile, it could cause eye infections or other issues when injected into the eye.
Who’s affected
People who have this compounded ophthalmic solution for eye injections. Those with eye conditions or recent eye surgery may be at slightly higher risk.
How to tell if you have this one
Look for the product name 'Ceftazidime Sterile Ophthalmic Solution for Injection Preservative Free 11.25mg / 0.5ml (22.5mg/ml) 0.5ml per syringe'. It was compounded by Edge Pharma, LLC and sold with lot number 02-2020-04@4.
- Brand
Edge Pharma- Category
Drug
What to do — step by step
Check Product Details
Verify the product name and lot number on the syringe to confirm if it's part of this recall.
Questions people ask
Is this product safe to use?
The recall states the sterility testing media was expired, so the solution may not be sterile. Do not use it until the recall is resolved.
How do I get a replacement?
The recall record does not specify a replacement process or remedy.
Is this product for home use?
This is a compounded drug for intraocular injection only, not for home use or resale.
Contact Edge Pharma
We’ve drafted a message you can send Edge Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0238-2021 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0238-2021 from Edge Pharma. 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.
Similar recalls
Keep exploring
From people who’ve dealt with this
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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-0238-2021 (March 19, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0238-2021 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.