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Policy version 2026-07-21, effective July 21, 2026.
United States
TerminatedClass II
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.
| Product description | UPC | Quantity | Lot / code information |
|---|---|---|---|
| Gourmet Apple Spice Monster Muffins (4 count) | Not published in this source record | 170,186 total units | UPC # 2100867004000 |
This recall shares FDA event ID 74818 with 10 other product entries in Public Health Trace.
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
FDA Recall United States TerminatedTerminated: May 1, 2017Historical recordClass II
Responsible company: Weis Markets, Inc., Ice Cream Division
FDA Recall United States TerminatedTerminated: September 29, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: September 29, 2024Historical recordClass II
FDA Recall United States TerminatedTerminated: September 29, 2024Historical recordClass II
A map highlighting the states named in the source's distribution description.
Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.
| State | Distributed |
|---|---|
| Pennsylvania | 1 |
| New Jersey | 1 |
| New York | 1 |
| Maryland | 1 |
| Virginia | 1 |
States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.
View FDA enforcement record -- the specific openFDA record this summary was built from.
This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.
FDA Enforcement Reports -- FDA's general, official recall and enforcement information.
View raw source data -- the machine-readable record this page's information was built from.
Retrieved by Public Health Trace:
A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.
According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.
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