Parker Laboratories recalls Redux Electrolyte Creme (Product Ref. 66-04) due to low viscosity. This may cause product to spread too easily, but no specific safety risks are described in the recall notice.
Product demonstrates low viscosity.
Parker Laboratories is recalling Redux Electrolyte Creme (Product Ref. 66-04) because it has low viscosity. This means the product may spread too easily, but the recall does not mention any safety risks or injuries. Consumers are not instructed to stop using or return the product.
The product has low viscosity, meaning it spreads easily. However, the recall does not specify how this could cause harm or what safety risks might exist. No injuries or serious hazards are mentioned in the notice.
Anyone who owns or uses the Redux Electrolyte Creme (Product Ref. 66-04) from Parker Laboratories. The product is not likely to pose a risk to most users since no safety hazards are described.
Check for the product name 'Redux Electrolyte Creme' with Product Reference 66-04. The unique identifiers include UDI: 20855683006399 (Master), 10855683006392 (Inner Box), 00855683006395 (Each).
Look for the Product Reference 66-04 on the packaging or label.
The recall states the product has low viscosity but does not describe any safety risks or injuries. No specific hazards are mentioned.
The recall does not instruct users to stop using or return the product. No action is required based on the notice.
The recall does not provide any action steps. Consumers are not told to discard, repair, or take other steps.
We’ve drafted a message you can send Parker Laboratories to request your refund or repair — edit it as you like.
Subject: Recall Z-1604-2024 — Parker Laboratories Parker Laboratories Hello, I own a Parker Laboratories that is covered by recall Z-1604-2024 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.
