Sunstar recalls 16 fl oz Butler Clear Dip due to Burkholderia contaminans risk. Affected lots: 532952, 535180, 536513, 536514, 53948:551038, 551039. Stop using if contaminated.
“Sunstar Butler Clear Dip Recall: Contamination Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/62992-sunstar-butler-clear-dip-recall-contamination-risk. Based on FDA recall #Z-1382-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1382-2021%22&limit=1).
The FDA announced on March 23, 2021, that Sunstar Americas, Inc. voluntarily recalled SUNSTAR Butler Clear Dip, 16 FL OZ, SKU #716PA, due to potential contamination with Burkholderia contaminans. The recall affects 19,471 bottles distributed in the U.S., Taiwan, Thailand, Malaysia, Japan, Hong Kong, and Mexico.
Lot Numbers: 532952, 535180, 536513, 536514, 539487, 551038, 551039
The hazard
The product may be contaminated with Burkholderia contaminans. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Sunstar Americas, Inc. has 5 other recalls on record since October 27, 2020. Other recent recalls of similar products include Cardinal Health Presource Packs with Contaminated Wipes Recalled (July 29, 2026), Windstone Medical Preop Kit-NS Recall (May 21, 2026), and Medline Convenience Kits Recall (August 11, 2026).
How to tell if you have this one
Check the product label for the lot numbers: 532952, 535180, 536513, 536514, 539487, 551038, or 551039. The product is a 16 fl oz Butler Clear Dip with SKU #716PA.
Brand
Sunstar
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Lot Number
Look for the lot numbers on the label: 532952, 535180, 536513, 536514, 539487, 551038, or 551039.
Discard Contaminated Product
If the product has one of the listed lot numbers, discard it immediately to avoid potential health risks.
How this recall unfolded
Recall timeline
FDA terminated this recall 2.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-1382-2021 (March 23, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1382-2021 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.