Recall record at a glance
| Official record | F-0179-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Terminated |
| Recalling firm | Treehouse Foods |
| Report date | Dec 4, 2024 |
| Recall initiation date | Oct 17, 2024 |
| Quantity | 9,907,389 cases (total) |
| Location | Oak Brook, IL, United States |
Official product description
DUNCAN HINES 1/3.12kg GRDL WFL BLGN ORIG 4IN - DUNHN UPC 091479060275 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151903331 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG-KRSMX UPC 00686151805307 KRUSTEAZ 1/3.44lb GRDL WFL BLGN ORIG - KRSTZ UPC 686151904017 GORDON CHOICE 1/3.12kg GRDL WFL BLGN ORIG - GDNCH UPC 00620868161745 PRESIDENT'S CHOICE 12/390g GRDL WFL BLGN ORIG - PCHOI UPC 060383035549 BEST CHOICE 12/13.75oz GRDL WFL BLGN ORIG - BSTCH UPC 070038644019 GOOD & GATHER 12/13.75oz GRDL WFL BLGN ORIG-GDGTR UPC 085239157947 GIANT EAGLE 12/13.75oz GRDL WFL BLGN ORIG-GT/EG UPC 030034011680 H-E-B 12/13.75oz GRDL WFL BLGN ORIG-HEBUT UPC 041220908271 PRIVATE SELECTION 12/13.75oz GRDL WFL BLGN ORIG-PRVSN UPC 011110893994 SE GROCERS 12/13.75oz GRDL WFL BLGN ORIG - SEGGR UPC 038259117163 WEGMANS 12/13.75oz GRDL WFL BLGN ORIG-WEGMN UPC 077890550342 COMPLIMENTS 12/390g GRDL WFL BLGN ORIG-CMPLM UPC 055742347173 KRUSTEAZ 12/13.75oz GRDL WFL BLGN ORIG-KRSTZ UPC 686151903355 CULINARY TOURS 12/13.75oz GRDL WFL BLGN ORIG - CLNTR UPC 011225148552 PUBLIX 12/13.75oz GRDL WFL BLGN-PUBLX UPC 041415204546 SIGNATURE SELECT 8/13.75oz GRDL WFL BLGN ORIG-SIGSL UPC 021130095575 WEGMANS 12/13.75oz GRDL WFL BLGN ORIG- WEGMN UPC 077890550342
Why the product was recalled
potential to be contaminated with Listeria monocytogenes
Distribution information
Nationwide in USA and Canada
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.