Sunstar Butler Clear Dip 12-bottle case recall: Product lacks premarket clearance
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.
Lower-risk recall
Product lacks premarket clearance.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/61260-sunstar-butler-clear-dip-12-bottle-case-recall-product-lacks.
Source Summary by GovInfoNow · govinfonow.com/recall/61260-sunstar-butler-clear-dip-12-bottle-case-recall-product-lacks · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0720-2022
Cite this page
“Sunstar Butler Clear Dip 12-bottle case recall: Product lacks premarket clearance.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/61260-sunstar-butler-clear-dip-12-bottle-case-recall-product-lacks. Based on FDA recall #Z-0720-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0720-2022%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
Check for the SKU 716P (Clear Dip : 16oz) and lots S350LP, S350LN, T116JA, T117JE, T187DH, T187DJ, or T263FD on the product label.
- Brand
Sunstar- Category
Medical device
What to do — step by step
Check Product Details
Identify if your Butler Clear Dip 12-bottle case has the SKU 716P and the listed lots.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “United States Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 19 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-0720-2022 (January 14, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0720-2022 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.