Ecometics AstrinGyn Vials Recall: CGMP Deviations Risk

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Contact the company & request your remedy

Recalling firmEcometics, Inc.19 Concord St, N/A · Norwalk, CT 06854-3706

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Ecometics is recalling AstrinGyn vials that were manufactured without following current good manufacturing practices. This could mean the product is unsafe, but the recall does not include a specific fix or return process.

Why it’s dangerous

The product was made without following current good manufacturing practices. This could lead to unsafe product quality, but the exact risk is not specified in the recall notice.

Who’s affected

Women using AstrinGyn vials for medical purposes may be affected. Those with the specific lot numbers listed are at risk.

How to tell if you have this one

Check the lot number on the vial: 2E144A, 2E157A (expiring 11/2023), 2E270A (expiring 3/2024), or 2E300A (expiring 4/2024). The product was sold with NDC 59365-6065-0.

Brand
Ecometics
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Lot Number
Look for lot numbers 2E144A, 2E157A, 2E270A, or 2E300A on the vial label.

✎ GovInfoNow

Questions people ask

Is there a fix for these vials?

The official recall notice does not specify any remedy or action to take.

What should I do if I have these vials?

The recall does not include a specific remedy, so no action is required beyond checking the lot number.

When were these vials manufactured?

The vials were manufactured with specific lot numbers that expire by 11/2023, 3/2024, or 4/2024.

Take action

Contact Ecometics

We’ve drafted a message you can send Ecometics to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall D-1101-2023 — Ecometics Ecometics

Hello,

I own a Ecometics that is covered by recall D-1101-2023 from Ecometics.

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-1101-2023 (August 9, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-1101-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.

Ecometics, Inc. recalls AstrinGyn (Ferric Subsulfate) Aqueous, 259 mg/g, 8 gm Single Use Vials, Manufactured for CooperSurgical, Trumbull, CT

Recall notice