Homeocare Laboratories recalls DoloEar Earache Drops due to cGMP deviations. Affected lots expire Nov-24 or Apr-25. Consumers should check labels for NDC 55758-001-15.
cGMP deviations
Homeocare Laboratories is recalling DoloEar Earache Drops bottles that were distributed by Pharmadel LLC. The recall is due to cGMP deviations, which means the product may not meet quality standards.
cGMP deviations refer to failures in manufacturing quality control processes. This could mean the product does not meet safety and quality standards, but the specific risk to consumers is not clearly described in the recall notice.
People who own or use DoloEar Earache Drops bottles with NDC 55758-001-15, distributed by Pharmadel LLC. Those who have the product with expiration dates Nov-24 or Apr-25 are most at risk.
Check for DoloEar Earache Drops bottles labeled with NDC 55758-001-15. The product was distributed by Pharmadel LLC and has expiration dates Nov-24 or Apr-25.
Look for the NDC code 55758-001-15 and expiration dates Nov-24 or Apr-25 on the bottle.
The recall is due to cGMP deviations, which are failures in manufacturing quality control processes.
The official notice does not specify a remedy, so check the product label for the NDC code and expiration dates.
Look for DoloEar Earache Drops bottles with NDC 55758-001-15 and expiration dates Nov-24 or Apr-25.
We’ve drafted a message you can send Homeocare to request your refund or repair — edit it as you like.
Subject: Recall D-0884-2023 — Homeocare Homeocare Hello, I own a Homeocare that is covered by recall D-0884-2023 from Homeocare. 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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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.
