Parker Laboratories recalls Helix CBD Clinical Cream (Menthol 7.4%) due to CGMP deviations. Products packaged in 3 gm pouches (NDC 30775-054-01) and 2 fl. oz. tubes (NDC 30775-054-02) may be affected.
CGMP Deviations
Parker Laboratories is recalling Helix CBD Clinical Cream (Menthol 7.4%) because of CGMP deviations. This means the product may not meet quality standards, though the specific risk is not detailed in the recall.
CGMP deviations refer to failures in the manufacturing process that could affect product quality. However, the recall does not specify what the exact risk is or how it might impact users.
People who own or use Helix CBD Clinical Cream (Menthol 7.4%) packaged in 3 gm pouches (NDC 30775-054-01) or 2 fl. oz. tubes (NDC 30775-054-02) are affected. Those with the product may be at risk due to potential quality issues.
Check for Helix CBD Clinical Cream (Menthol 7.4%) in 3 gm pouches (NDC 30775-054-01) or 2 fl. oz. tubes (NDC 30775-054-02). The product may have lot numbers J1121011 (exp. 12/21/2023) or A0921009/A0921008 (exp. 8/18/2023).
Look for the product name, packaging size, and lot number to confirm if it's recalled.
The recall states CGMP deviations, which means manufacturing quality issues, but does not specify the exact risk.
Check for Helix CBD Clinical Cream (Menthol 7.4%) in 3 gm pouches (NDC 30775-054-01) or 2 fl. oz. tubes (NDC 30775-054-02) with lot numbers J1121011 (exp. 12/21/2023) or A0921009/A0921008 (exp. 8/18/2023).
The recall does not specify a remedy, so check with Parker Laboratories for further instructions.
We’ve drafted a message you can send Parker Laboratories to request your refund or repair — edit it as you like.
Subject: Recall D-1093-2023 — Parker Laboratories Parker Laboratories Hello, I own a Parker Laboratories that is covered by recall D-1093-2023 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.
