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CriticalFDAfda-F-1734-2012SALMONELLA CONTAMINATION

Product is labeled in part: "***LEASA Living Alfalfa Sprouts***CHOLESTEROL FREE***PRESERVATIVE FREE***KEEP REFRIGERATED***NET WT. 6 OZ. ...

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (Salmonella contamination). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
433
Recall Date
June 20, 2012
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1734-2012.

LEASA Industries Co., Inc. initiated a recall of 6 OZ containers of LEASA Living Alfalfa Sprouts with Use By Date 07/02/2012, UPC 75465-55912 after being informed by the Florida Department of Agriculture and Consumer Safety that a product sample had tested positive for Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1734-2012.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Leasa Industries Co., Inc. or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. 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-1734-2012.

LEASA Industries Co., Inc.

FDA

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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.

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Leasa Industries Co., Inc. Recall FAQ

Leasa Industries Co., Inc. is the subject of a food safety report: Product is labeled in part: "***LEASA Living Alfalfa Sprouts***CHOLESTEROL FREE***PRESERVATIVE FREE***KEEP REFRIGERATED***NET WT. 6 OZ. .... The notice was published on June 20, 2012 by the U.S. Food and Drug Administration (FDA). Approximately 433 units are potentially affected.