CLASS IIFood recall · Reported 19 Oct 2016 · FDA Enforcement Report
Gourmet Cranberry Orange Monster Muffins recalled
Weis Markets, Inc., Ice Cream Division is recalling Gourmet Cranberry Orange Monster Muffins, distributed in Maryland, New Jersey, New York, Pennsylvania, Virginia. The recall was initiated on 21 Jul 2016 and the FDA has classified it as Class II.
Check your package
Lot, batch or date codesUPC # 2100907004007
Quantity recalled170,186 total units
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
WEIS MARKETS IS ISSUING A VOLUNTARY RECALL FOR 30 BAKERY PRODUCTS INCLUDING MUFFINS, COOKIES, AND SHORTBREAD AND BAKED BREAD ITEMS DUE TO THE POTENTIAL PRESENCE OF SMALL METAL FRAGMENTS (2-9MM) IN THE SUGAR TOPPING USED ON THESE PRODUCTS. THE VOLUNTARY ACTION IS BEING TAKEN DUE TO OUR SUPPLIERS RECALL OF THE SUGAR INGREDIENT.
Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.
WEIS MARKETS IS ISSUING A VOLUNTARY RECALL FOR 30 BAKERY PRODUCTS INCLUDING MUFFINS, COOKIES, AND SHORTBREAD AND BAKED BREAD ITEMS DUE TO THE POTENTIAL PRESENCE OF SMALL METAL FRAGMENTS (2-9MM) IN THE SUGAR TOPPING USED ON THESE PRODUCTS. THE VOLUNTARY ACTION IS BEING TAKEN DUE TO OUR SUPPLIERS RECALL OF THE SUGAR INGREDIENT.
Which lots are affected?
UPC # 2100907004007
Where was it sold?
Products were distributed to: PA,NJ,NY,MD,VA
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.