Skip to main content
RecallFDAfda-F-1408-2015OTHER

Weis Veggie Sticks Net Wt. 6 oz. Packed For Weis Markets, Inc. Sunbury, PA 17801 With code dates: 10 Dec 2014 thru 7 Apr 2015 Natu...

Category
Units Affected
13,162
Recall Date
December 16, 2014
Issuing Agency
Hazard
Other

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1408-2015.

Firm's sodium claims of 55 g/serving is incorrect. Product analyzed and found to contain shows 260 - 290 mg/serving size

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-1408-2015.

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 Keystone Food Products 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-1408-2015.

Keystone Food Products Inc

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

Keystone Food Products Inc Recall FAQ

Keystone Food Products Inc is the subject of a food safety report: Weis Veggie Sticks Net Wt. 6 oz. Packed For Weis Markets, Inc. Sunbury, PA 17801 With code dates: 10 Dec 2014 thru 7 Apr 2015 Natu.... The notice was published on December 16, 2014 by the U.S. Food and Drug Administration (FDA). Approximately 13,162 units are potentially affected.