Edge Pharma, LLC recalls Vancomycin HCL 1.5 mg Edge Pharma, LLC 856 Hercules Dr. Colchester, VT 05446 NDC 05446-1458-01
Edge Pharma recalls Vancomycin HCL 1.5mg (NDC 05446-1458-01) due to labeling error on declared strength. Affected units may have incorrect dosage information.
Lower-risk recall
Labeling: Label Error on Declared Strength
Contact the company & request your remedy
What happened, in plain English
Edge Pharma is recalling a specific batch of Vancomycin HCL 1.5mg tablets because the label shows an incorrect declared strength. This could lead to improper dosing if the medication is used without verifying the correct strength. Read more at govinfonow.com/recall/36973-edge-pharma-vancomycin-hcl-1-5mg-label-strength-error-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/36973-edge-pharma-vancomycin-hcl-1-5mg-label-strength-error-recall · Updated October 5, 2026 · FDA enforcement record: FDA #D-1562-2020
Cite this page
“Edge Pharma Vancomycin HCL 1.5mg: Label Strength Error Recall.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/36973-edge-pharma-vancomycin-hcl-1-5mg-label-strength-error-recall. Based on FDA recall #D-1562-2020 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1562-2020%22&limit=1).
Why it’s dangerous
The label error means the declared strength on the medication might not match the actual strength. This could result in incorrect dosing if the medication is used without verifying the correct strength. However, the recall does not indicate a risk of serious injury or death.
Who’s affected
Patients who have received this specific batch of Vancomycin HCL 1.5mg tablets (NDC 05446-1458-01) from Edge Pharma. Healthcare providers using this medication are also affected.
How to tell if you have this one
Check for the product name 'Vancomycin HCL 1.5mg' with NDC code 05446-1458-01. The batch lot number is 06-2020-04@2 and the expiration date is 09-16-2020.
- Brand
Edge Pharma- Category
Drug
What to do — step by step
Check Product Label
Verify the NDC code 05446-1458-01 and lot number 06-2020-04@2 on the medication label.
Questions people ask
Is this recall dangerous?
No, the recall is for a labeling error that could lead to incorrect dosing, but it does not pose a risk of serious injury or death.
How do I know if I have this product?
Check for the NDC code 05446-1458-01 and lot number 06-2020-04@2 on the medication label.
What should I do if I have this product?
The recall does not specify a remedy, so you should check the label and 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-1562-2020 — Edge Pharma Edge Pharma Hello, I own a Edge Pharma that is covered by recall D-1562-2020 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-1562-2020 (July 2, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1562-2020 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.