Atlantic Management Resources Ltd. recalls ProSiron: Calendula Oil homeopathic formula in 1/8 fl oz bottles due to cGMP deviations. No remedy specified in official notice.
cGMP Deviations
Atlantic Management Resources Ltd. is recalling ProSirona, a homeopathic formula containing Calendula Oil, because of manufacturing quality control issues. This recall does not include a specific remedy or action for consumers.
The recall is due to cGMP (current Good Manufacturing Practice) deviations, which means the product was made without following proper quality control standards. This could potentially affect the safety and effectiveness of the product, but the specific risk to consumers is not clearly described in the notice.
People who purchased ProSirona homeopathic formula in 1/8 fl oz bottles from Endometriosis Assoc. distributors. Those with endometriosis or using homeopathic remedies may be at higher risk.
Check for ProSirona homeopathic formula in 1/8 fl oz (3.5 g) bottles with lot code B-02. The product was distributed by Endometriosis Assoc. and manufactured by Claire Ellen Topicals.
Look for the lot code B-02 on the product label to confirm if it's recalled.
No remedy is specified in the official recall notice.
cGMP deviations refer to failures in current Good Manufacturing Practices, which are quality control standards for products. The exact nature of the deviation is not described in this recall.
Check for ProSirona homeopathic formula in 1/8 fl oz (3.5 g) bottles with lot code B-02 distributed by Endometriosis Assoc.
We’ve drafted a message you can send Atlantic Management Resources Ltd. to request your refund or repair — edit it as you like.
Subject: Recall D-0083-2023 — Atlantic Management Resources Ltd. Atlantic Management Resources Ltd. Hello, I own a Atlantic Management Resources Ltd. that is covered by recall D-0083-2023 from Atlantic Management Resources Ltd.. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.