Consumer Product Partners recalls Spectrum Advanced Gel Hand Sanitizer with 70% ethyl alcohol that tests below label claim due to cloudy appearance. Affected units have specific NDC and lot numbers.
Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol
Consumer Product Partners is recalling Spectrum Advanced Gel Hand Sanitizer because it has a cloudy appearance and tests below the claimed 70% ethyl alcohol content. This means the product may not effectively sanitize hands as advertised, potentially reducing its protective benefits.
The product has a cloudy appearance and tests below the labeled 70% ethyl alcohol concentration. This indicates the sanitizer may not provide the intended level of protection against germs, making it less effective for hand hygiene.
People who purchased the Spectrum Advanced Gel Hand Sanitizer with the specific NDC number 53329-202-08 and lots 0644682 or 0644683 are affected. Those using the product for hand hygiene are most at risk of reduced effectiveness.
Check for the NDC number 53329-202-08 and lot numbers 0644682 (expiring November 14, 2026) or 0644683 (expiring November 16, 2026) on the product label.
Look for the NDC number 53329-202-08 and lot numbers 0644682 or 0644683 on the product label.
The product has a cloudy appearance and tests below the labeled 70% ethyl alcohol content, meaning it may not effectively sanitize hands as advertised.
Check for the NDC number 53329-202-08 and lot numbers 0644682 (expiring November 14, 2026) or 0644683 (expiring November 16, 2026) on the product label.
The recall record does not specify a remedy, so no action is required beyond checking the product label.
We’ve drafted a message you can send Consumer Product Partners to request your refund or repair — edit it as you like.
Subject: Recall D-0458-2025 — Consumer Product Partners Consumer Product Partners Hello, I own a Consumer Product Partners that is covered by recall D-0458-2025 from Consumer Product Partners. 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.
