Parker Laboratories recalls Helix CBD Therapy Cream (Menthol 7.4%) due to CGMP deviations. Products with specific NDC codes and expiration dates are affected. Consumers should contact the company for details.
CGMP Deviations
Parker Laboratories is recalling Helix CBD Therapy Cream (Menthol 7.4%) because of CGMP deviations. This means the product may not meet quality standards, though the exact risk isn't specified in the recall notice.
CGMP deviations refer to failures in the manufacturing process that could affect product safety and quality. However, the recall notice does not specify the exact nature of the deviations or the potential risks to consumers.
Anyone who owns or uses the Helix CBD Therapy Cream with the listed NDC codes and expiration dates. People using the product for medical purposes may be at higher risk due to potential quality issues.
Check for the product names and NDC codes: 3 g pouch (NDC 30775-053-01), 2 fl. oz. tubes (NDC 30775-053-02), or 4 fl. oz. tubes (NDC 30775-053-04). The expiration dates are 12/16/2023 for the 3 g pouch and 8/16/2023 for the tubes.
Identify the NDC code and expiration date on the product packaging to confirm if it is affected.
The recall is due to CGMP deviations, which indicate potential quality issues in manufacturing, though the exact risk is not specified.
The recall notice does not provide specific action steps beyond checking product details. Contact Parker Laboratories for further instructions.
The recall notice does not describe specific safety risks, so the exact danger level is unknown.
We’ve drafted a message you can send Parker Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-1092-2023 — Parker Laboratories Parker Laboratories Hello, I own a Parker Laboratories that is covered by recall D-1092-2023 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.
