Recall record at a glance
| Official record | F-0517-2014 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Garden-Fresh Foods, Inc. |
| Report date | Dec 11, 2013 |
| Recall initiation date | Oct 30, 2013 |
| Quantity | 1,159,754.46 total pounds, for all varieties |
| Location | Milwaukee, WI, United States |
Official product description
Family Style Macaroni Salad, Product Code 0 11596 52060 5, 2/5 lb; Garden-Fresh Macaroni Salad,Product Code 0 11596 52005 6, 2/5 lb; Garden-Fresh Macaroni Salad, Product Code 0 11596 14018 6, 12/16 oz; Garden-Fresh Macaroni Salad, Product Code 0 11596 24210 1, 8/2 lb; Garden-Fresh Macaroni Salad, Product Code 0 11596 34305 1, 6/3 lb; Grandpas Macaroni Salad, Product Code 0 11596 14066 7, 12/16 oz; Grandpas Macaroni Salad, Product Code 0 11596 52066 7, 2/5 lb; Weis Original Macaroni Salad,Product Code 0 41497 05839 6, 12/16 oz; Weis Original Macaroni Salad, Product Code 0 41497 05904 1, 4/3 lb; Weis Original Macaroni Salad, Product Code 0 11596 52106 0, 2/5 lb; Finest Traditions Macaroni Salad, Product Code 10 733147 10286 9, 1/8 lb; Finest Traditions Macaroni Salad, Product Code 7 33147 00018 2, 6/16 oz; Rogges Macaroni Salad, Product Code 0 11596 52019 3, 2/5 lb; Dairy Fresh Macaroni Salad, Product Code 0 70163 56415 2, 2/5 lb; Spartan Macaroni Salad, Product Code 0 11213 90321 7, 6/16 oz; Market Pantry Macaroni Salad, Product Code 0 85239 24105 9, 6/16 oz.
Why the product was recalled
Garden-Fresh Foods is recalling various ready-to-eat salads, slaw, and dip products sold under various brands and codes because they may be contaminated with Listeria monocytogenes.
Distribution information
CA, IL, IN, MA, MI,MN, MO, OH, PA, WI.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.
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
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