MDM 10200921 Natural and Artificial Lemon Flavored Poppy Seed Muffin
Reason Frozen, unbaked muffins potentially contaminated with small pieces of plastic.
MDM 10200917 Double Dutch Muffin recall
Recalled by Brill, Inc., a CSM Bakery Solutions Company - Atlanta Ingredients · Tucker, GA, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Frozen, unbaked muffins potentially contaminated with small pieces of plastic.
Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.
What was recalled
48533 MDM 10200917, Double Dutch Muffin, pre - deposited - unbaked - keep frozen, UPC 10035074485337, Net Wt. 25.3 lbs, Manufactured by CSM Bakery Products NA, Inc. Tucker, GA
Quantity: 320 cases
Food: Bread & bakery
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.
Batch# 1000686280, Best By Date 12/29/2019
Where it was sold
California Iowa Massachusetts Minnesota New Jersey Pennsylvania Utah
FDA's distribution note: Distributed to grocery store distribution centers in CA, IA, MA, MN, PA, NJ, and UT for baking in baking departments of retail grocery stores.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
- Brill, Inc., a CSM Bakery Solutions Company - Atlanta Ingredients
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 12, 2019
- In FDA report of
- Aug 14, 2019
- Terminated
- Sep 16, 2019
- FDA recall number
- F-1982-2019 · event 83364
- 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.
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