FDA recall record

Lake Michigan Distilling Co Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol recall — FDA F-1536-2018

Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a voluntary recall of Ethanol Extraction s 190 Proof Non-Denatured Grain Alcohol due…

Class Iclassification
F-1536-2018official record ID
Jun 13, 2018report date

Recall record at a glance

Official recordF-1536-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmLake Michigan Distilling Co LLC
Report dateJun 13, 2018
Recall initiation dateMay 22, 2018
QuantityApproximately 900 Gallons was distilled and sold
LocationLa Porte, IN, United States

Official product description

Ethanol Extraction 190 Proof Non-Denatured Grain Alcohol, Multiple sizes: 8 oz, 16 oz, 32 oz, 64 oz, 1 gal, 2.5 gals, 5 gals, 55 gallon drum, 8oz clear PVC cylinder bottles, all others heavy-duty polyethylene bottles (except single 55-gallon plastic drum).

Why the product was recalled

Lake Michigan Distilling, LLC, dba Ethanol Extraction has initiated a voluntary recall of Ethanol Extraction s 190 Proof Non-Denatured Grain Alcohol due to contamination with methanol which could cause serious injury or death if consumed.

Distribution information

Domestic: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MT, NC ,ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, TN, TX, UT, VA, VI, VT, WA, WI , WV, WY Foreign: VI

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Press Release.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.