Meijer Plain Knot Rolls
Reason R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer Plain Knot Rolls" and 8 ct. packages of Assorted Dinner Rolls 128 ct. because they may contain trace amounts of undeclared peanuts.
Assorted Dinner Rolls recall
Recalled by R.W. Bakers Co. Inc. · Norton Shores, MI, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
R.W. Bakers Co. of Muskegon, MI, is recalling its 8 ct. packages of "Meijer Plain Knot Rolls" and 8 ct. packages of Assorted Dinner Rolls 128 ct. because they may contain trace amounts of undeclared peanuts.
Undeclared allergen: Peanut
For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.
What was recalled
Assorted Dinner Rolls, 128 ct., Net Wt. 10.2 lbs; 16/ 8 ct./case
Quantity: 47 cases
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.
The lot number is 16041 with a production date of 2/10/16; Product number 4180. This information is found on the master case of the product. This product does not have a UPC number
Where it was sold
Illinois Indiana Kentucky Michigan Ohio Virginia Wisconsin
FDA's distribution note: Domestic: MI, OH, WI, KY, IN, IL Foreign: None; VA/DOD: None
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. The risk from an undeclared allergen is to people allergic to peanut; for anyone else the product is generally not a safety concern. 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
- R.W. Bakers Co. Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Mar 28, 2016
- In FDA report of
- May 11, 2016
- Terminated
- Feb 10, 2017
- FDA recall number
- F-1307-2016 · event 73700
- 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.