Report cards › Food › R.A.B. Food Group, LLC

MANISCHEWITZ

Owned by R.A.B. Food Group, LLC · 199 products in USDA FoodData Central · as of Oct 28, 2026 · Report an error · Change log

CSWH grade B (81)

Method v1.0 (how we grade), based on the records below; exact score 80.9849.

Grade by indicator
IndicatorGradeWhat we found
Recalls (40%)C (60)1 Class I (10 points) · 1 event For current recalls see FDA and USDA.
Ingredients (40%)A (92)Tier A: 0 of 199 products · A (100) (25%)
Tier B: 24 of 199 products (Partially hydrogenated oil (PHO), FD&C Yellow No. 5, FD&C Blue No. 1, FD&C Red No. 40, Titanium dioxide, Certified food colors (any FDA batch-certified color, incl. lakes) and 1 more) · B (80) (15%) · products
FDA warning letters (20%)A (100)None found to the owner Oct 28, 2021 to Oct 28, 2026.

Shown, not graded: recall reasons (1 undeclared allergen) · IARC notes (0 products) · FDA dye pledge: none on FDA's tracker.

Recalls, Oct 28, 2021 to Oct 28, 2026

  1. Class I, Dec 1, 2023 · Undeclared allergen · FDA event 93518

    • Manischewitz Magic Max's Dark Chocolate Coins, NET WT. 0.53 OZ (15g), UPC: 072700200387 Display Box UPC: 072700200356, 12 bags per case. Product packaged in gold foil in blue netting bags.

      Reason (FDA's words)
      Undeclared milk due to mispackaging
      Code information
      Lot 2283
      Recalling firm
      Kenover Marketing Corp.
      Dates
      Recall started Dec 1, 2023; classified Dec 15, 2023
      Status
      Terminated (status reported by FDA at classification)
      How we matched it
      matched by UPC 72700200387 (upc)

      FDA record F-0608-2024: openFDA · Report an error

Store-brand and co-packer recalls count on a brand only when a UPC in the recall matches one of its products.

Ingredients on our watch list

Products (24)

Labels change: each row shows the date of its FoodData Central record. A brand that has changed a recipe can report it with "Report an error".

FDA warning letters to R.A.B. Food Group, LLC, Oct 28, 2021 to Oct 28, 2026

None found from FDA food offices.

FDA notes that later events may have changed the regulatory status of what a letter discusses.