Homeocare Arnica 7 Cream Recall: C G M P Deviations

Take action

Contact the company & request your remedy

Recalling firmHomeocare Laboratories, Inc.7 Odell Plz Ste 142-146, N/A · Yonkers, NY 10701-1407

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

✎ GovInfoNow plain-language explainer

What happened, in plain English

Homeocare Laboratories is recalling Arnica 7 Cream (2 oz) because of manufacturing quality issues. This recall is due to cGMP deviations, which could impact product safety and quality.

Why it’s dangerous

cGMP deviations refer to manufacturing quality control failures. This could mean the product doesn't meet safety and quality standards, potentially affecting its effectiveness or safety.

Who’s affected

People who own or use Arnica 7 Cream (2 oz) with UPC 8 60208 00181 6, lot #2446, expiring March 2024. Those using the product for skin conditions may be at risk.

How to tell if you have this one

Check for the UPC 8 60208 00181 6 on the product label. The affected lot is #2446, expiring March 2024. This cream was manufactured for Brazmedics, LLC in New York.

Brand
Homeocare Laboratories
Category
Drug

Based on the official FDA remedy

What to do — step by step

Check Product Details
Look for UPC 8 60208 00181 6 and lot #2446 on the cream label.

✎ GovInfoNow

Questions people ask

Is this cream safe to use?

The recall is due to manufacturing quality issues, but the product may still be safe. Homeocare Laboratories has not provided specific safety details.

What should I do if I have this cream?

The recall record does not specify a remedy, so no action is required beyond checking if your product matches the details.

How can I confirm if my cream is affected?

Check for UPC 8 60208 00181 6 and lot #2446 on the label. The cream expires March 2024.

Take action

Contact Homeocare Laboratories

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

✉️ Open in email

Subject: Recall D-0881-2023 — Homeocare Laboratories Homeocare Laboratories

Hello,

I own a Homeocare Laboratories that is covered by recall D-0881-2023 from Homeocare Laboratories.

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

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-0881-2023 (June 5, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0881-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.

Homeocare Laboratories, Inc. recalls Arnica 7 Cream, net wt 2 oz (56.7g), Manufactured for: Brazmedics, LLC, New York, NY 10021 UPC 8 60208 00181 6

Recall notice