Sunstar recalls Butler Clear Dip 12-bottle cases with specific SKUs due to lack of premarket clearance. Consumers should check their product details to determine if affected.
Product lacks premarket clearance.
Sunstar is recalling Butler Clear Dip 12-bottle cases because they were not cleared by the FDA before being sold. This means the product may not meet safety standards, but it does not pose an immediate risk of injury.
The product lacks premarket clearance, meaning it was not reviewed by the FDA for safety before being sold. This could result in the product not meeting safety standards, but it does not cause immediate injury or health risks.
Owners of Butler Clear Dip 12-bottle cases with specific SKUs (716P) and lots listed in the recall are affected. People using these products for home or personal care are most at risk.
Check for the SKU 716P (Clear Dip : 16oz) and lots S350LP, S350LN, T116JA, T117JE, T187DH, T187DJ, or T263FD on the product label.
Identify if your Butler Clear Dip 12-bottle case has the SKU 716P and the listed lots.
No immediate danger is reported; the product lacks premarket clearance but does not cause injury or health risks.
Check the SKU 716P (Clear Dip 16oz) and lots S350LP, S350LN, T116JA, T117JE, T187DH, T187DJ, or T263FD on the label.
The recall does not specify a remedy, so no action is needed unless you want to check if your product is affected.
We’ve drafted a message you can send Sunstar to request your refund or repair — edit it as you like.
Subject: Recall Z-0720-2022 — Sunstar Sunstar Hello, I own a Sunstar that is covered by recall Z-0720-2022 from Sunstar. 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.
