Organic Coconut Butter, packaged in 16 oz. plastic jars, UPC 66016-40190 Oskri, 528 E. Tyranena Park Rd, Lake Mills, WI 53551. .
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (listeria). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0934-2019.
Sunflower and Tahini Butter has the potential to be contaminated with Listeria monocytogenes. EXPANDED1/21/2019 Recall was expanded to include all Oskri manufactured butters due to potential Listeria monocytogenes contamination.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0934-2019.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Oskri Corp. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- If you've been hurt by this product, report the incident to FDA.
Consumer Contact (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0934-2019.
Oskri Corp.
About the U.S. Food and Drug Administration
The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.
Visit FDA.gov →📣 Report a food, supplement, or cosmetic problem to the FDA
If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.
Oskri Corp. Recall FAQ
Oskri Corp. is the subject of a dairy safety report: Organic Coconut Butter, packaged in 16 oz. plastic jars, UPC 66016-40190 Oskri, 528 E. Tyranena Park Rd, Lake Mills, WI 53551. .. The notice was published on December 17, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 249,234 units are potentially affected.