Mrs. Miller's Homemade Jam Spicy Chili Bacon Jam packaged into
Reason Undeclared Allergen - Soy
Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam packaged into recall
Recalled by Mrs Millers Homemade Jams LLC. · Fredericksburg, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Undeclared Allergen - Soy
Undeclared allergen: Soy
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
Mrs. Miller's Homemade Jam Smokey BBQ Bacon Jam packaged into 9 oz glass jar 12 jars per case
Quantity: 5315 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.
All Smokey BBQ Bacon Jam are being recalled
Where it was sold
Alabama Arizona Delaware Florida Indiana Minnesota Mississippi North Carolina Ohio Pennsylvania Tennessee Virginia Vermont Wisconsin West Virginia
FDA's distribution note: AL, AZ, DE, IN, FL, NC, OH, MN, MS, PA, TN, VA, VT, WI, WV
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 soy; 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
- Mrs Millers Homemade Jams LLC.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 9, 2022
- In FDA report of
- Jun 1, 2022
- Terminated
- Jun 14, 2022
- FDA recall number
- F-1088-2022 · event 90170
- 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.