Weis Veggie Chips
Reason Firm's sodium claims of 55 g/serving is incorrect. Product analyzed and found to contain shows approx. 290 mg/serving size
Weis Veggie Sticks recall
Recalled by Keystone Food Products Inc · Easton, PA, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Firm's sodium claims of 55 g/serving is incorrect. Product analyzed and found to contain shows 260 - 290 mg/serving size
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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 Natures Place Veggie Straws Net Wt. 6 oz Distributed By: DZA Brands, LLC, Salisbury NC 28147/Scarborough, ME 04074 With code dates: 6 Jan 2015 thru 27 Apr 2015 Market Basket Veggie Sticks Net Wt. 6 oz Distributed by: DeMoulas Supermarkets, Inc. Tewksbury, MA 01876 With code dates: 2 Oct 2014 thru 8 Dec 2014
Quantity: 13,162 cs, 12 bags per case
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
10 Dec 2014 thru 7 Apr 2015 6 Jan 2015 thru 27 Apr 2015 2 Oct 2014 thru 8 Dec 2014
Where it was sold
Connecticut Massachusetts Maine New Hampshire New York Pennsylvania Rhode Island Vermont
FDA's distribution note: ME VT NH MA RI CT NY PA
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Keystone Food Products Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Dec 16, 2014
- In FDA report of
- Mar 18, 2015
- Terminated
- Aug 25, 2015
- FDA recall number
- F-1408-2015 · event 70067
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.