Acella Pharmaceuticals recalls 60-count cleansing pads with potential subpotent drug levels. These prescription pads may not contain enough active ingredient by end-of-shelf-life. Consumers should contact the manufacturer for details.
Subpotent drug: Out of specification for assay at the end-of-shelf-life 24-month period.
Acella Pharmaceuticals is recalling prescription cleansing pads that may have insufficient active ingredient by the end of their shelf life. This could mean the pads don't work as intended for treating wounds or infections.
The pads may have lower than expected drug levels by the end of their shelf life. This could mean they don't effectively treat wounds or infections as intended. However, the risk is only for the specific lot numbers and expiration date.
Prescription users who purchased the 60-count cleansing pads with lot numbers 21084 or 21085 expiring June 30, 2023. People using these pads for wound care are most at risk.
Check for lot numbers 21084 or 21085 on the packaging. The product is a prescription-only cleansing pad with a net weight of 3.7g per pad, sold in 60-count cartons.
Look for lot numbers 21084 or 21085 on the packaging to confirm if the product is recalled.
The product may have lower than expected drug levels by the end of its shelf life, which could affect its effectiveness for wound care.
Check for lot numbers 21084 or 21085 on the packaging. The product is a prescription-only cleansing pad with a net weight of 3.7g per pad in 60-count cartons.
The recall record does not specify a remedy, so contact Acella Pharmaceuticals for further instructions.
We’ve drafted a message you can send Acella Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0074-2023 — Acella Pharmaceuticals Acella Pharmaceuticals Hello, I own a Acella Pharmaceuticals that is covered by recall D-0074-2023 from Acella Pharmaceuticals. 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.
