Edge Pharma, LLC recalls Epinephrine/Lidocaine HCl, Sterile Ophthalmic Solution for Injection, 0.8 mL per syringe, Single Use Syringe,
Edge Pharma recalls sterile ophthalmic solution for injection with missing lot or expiration date. This affects prescription-only 0.8mL syringes sold in 2020. Contact for replacement.
Lower-risk recall
Labeling: Incorrect or Missing Lot and/or Exp Date
Contact the company & request your remedy
What happened, in plain English
Edge Pharma is recalling a prescription-only eye drop solution because it may lack a lot number or expiration date. This could lead to using expired or incorrect medication, which might cause eye injury or infection. Read more at govinfonow.com/recall/36570-edge-pharma-epinephrine-lidocaine-solution-recall-missing-lot-exp-date.
Source Summary by GovInfoNow · govinfonow.com/recall/36570-edge-pharma-epinephrine-lidocaine-solution-recall-missing-lot-exp-date · Updated October 4, 2026 · FDA enforcement record: FDA #D-0307-2021
Cite this page
“Edge Pharma Epinephrine/Lidocaine Solution Recall: Missing Lot/Exp Date.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/36570-edge-pharma-epinephrine-lidocaine-solution-recall-missing-lot-exp-date. Based on FDA recall #D-0307-2021 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0307-2021%22&limit=1).
Why it’s dangerous
The solution may not have a correct lot number or expiration date. This could mean the medication is expired or not properly tracked, increasing the risk of eye injury or infection if used incorrectly.
Who’s affected
Prescription holders of this eye drop solution are most at risk. The product is only available through medical providers and requires a prescription.
How to tell if you have this one
Check for the lot number and expiration date on the label. The product has NDC 05446-0863-01 and was sold with lot #10-2020-13 expiring 12/03/2020.
- Brand
Edge Pharma- Category
Drug
What to do — step by step
Check Label
Look for the lot number and expiration date on the product label.
Questions people ask
Is this product safe to use?
The product may not have a correct lot number or expiration date, so it should not be used until the label is verified.
How do I know if I have this product?
This product has NDC 05446-0863-01 and was sold with lot #10-2020-13 expiring 12/03/2020.
What should I do if I have this product?
Check the label for the lot number and expiration date. If missing, contact your healthcare provider for guidance.
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-0307-2021 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-0307-2021 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.
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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-0307-2021 (December 22, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0307-2021 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.