Brassica Pharma recalls Lubricant PM Ointment (3.5g tubes) due to lack of sterility assurance. Affected lots expire June 2024, May 2025, or September 2025. No remedy specified in official notice.
Lack of Assurance of Sterility
Brassica Pharma is recalling Lubricant PM Ointment tubes that may not be sterile. This could lead to infections if used improperly. The recall covers specific production lots with expiration dates through September 2025.
The ointment lacks proper sterility assurance, meaning it could contain harmful bacteria or other contaminants. If applied to broken skin or open wounds, this could cause infections. The risk is particularly concerning for medical use where sterility is critical.
People who own or use Lubricant PM Ointment tubes from Brassica Pharma with the specified lot numbers and expiration dates are affected. Those using the product for medical purposes are at higher risk due to potential infection.
Check the tube label for the lot numbers A2G01, A2G02 (expiring June 2024), A3F08, A3F09 (expiring May 2025), or A3J17, A3J18 (expiring September 2025). The product is packaged in 3.5 gram tubes distributed by AACE Pharmaceuticals.
Look for lot numbers A2G01, A2G02, A3F08, A3F09, or A3J17, A3J18 on the tube.
The recall states there is a lack of sterility assurance, which could lead to infections if used on broken skin or wounds. It is not safe to use without confirming it's not recalled.
The official notice does not specify a remedy, so contact Brassica Pharma directly for guidance on safe disposal or alternatives.
Check the tube label for lot numbers A2G01, A2G02 (expiring June 2024), A3F08, A3F09 (expiring May 2025), or A3J17, A3J18 (expiring September 2025).
We’ve drafted a message you can send Brassica Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0354-2024 — Brassica Pharma Brassica Pharma Hello, I own a Brassica Pharma that is covered by recall D-0354-2024 from Brassica 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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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.
