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CriticalFDAfda-F-1913-2017E COLI

20/20 LifeStyles Yogurt Peanut Crunch Bar. Bar UPC 7 8571 00052. Each bar has net weight 2 oz. Box UPC 7 8571 00053. Each box ha...

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
36,957
Recall Date
March 20, 2017
Issuing Agency
Hazard
E Coli

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1913-2017.

Product is recalled due to a potential contamination with E. coli O157:H7.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1913-2017.

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 Pro Sports Club 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-1913-2017.

Pro Sports Club

FDA

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.

How to report to FDAFile a report at FDA

Pro Sports Club Recall FAQ

Pro Sports Club is the subject of a dairy safety report: 20/20 LifeStyles Yogurt Peanut Crunch Bar. Bar UPC 7 8571 00052. Each bar has net weight 2 oz. Box UPC 7 8571 00053. Each box ha.... The notice was published on March 20, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 36,957 units are potentially affected.