Parker Laboratories recalls Helix Pain Relieving Cream (Menthol 7.4%) due to CGMP deviations. Products sold with specific NDC codes and expiration dates are affected. Consumers should check their product labels for the listed NDC numbers and expiration dates.
CGMP Deviations
Parker Laboratories is recalling Helix Pain Relieving Cream (Menthol 7.4%) because of CGMP deviations. This means the product may not meet quality standards and could pose a risk to consumers.
CGMP deviations refer to failures in the manufacturing process that could affect product quality. This may result in the cream not meeting safety and quality standards, potentially causing harm to users.
Anyone who owns or uses Helix Pain Relieving Cream with the listed NDC codes and expiration dates is affected. People using the product for pain relief are most at risk due to potential quality issues.
Check the product label for the NDC codes listed: 30775-051-01, 30775-051-03, 30775-051-04, 30775-051-12, 30775-051-32, 30775-051-50, 30775-051-95. Also look for the expiration dates associated with each product.
Look for the NDC codes and expiration dates listed in the recall notice to confirm if your product is affected.
Parker Laboratories is recalling Helix Pain Relieving Cream due to CGMP deviations, which means the product may not meet quality standards.
Products with specific NDC codes and expiration dates listed in the recall notice are affected.
Check the product label for the NDC codes and expiration dates provided in the recall notice.
We’ve drafted a message you can send Parker Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-1090-2023 — Parker Laboratories Parker Laboratories Hello, I own a Parker Laboratories that is covered by recall D-1090-2023 from Parker Laboratories. 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.
