FDA recall record

Fairfield Gourmet Food Corp d/b/a David's Markside Ultimate Peanut Butter Chocolate Cake, 7 recall — FDA F-0010-2024

Fairfield Gourmet Food Corp. d/b/a David s Cookies ,28 Industrial Road, Fairfield NJ 07004has initiated a recall of Markside Ultimate Peanut Butter…

Class IIclassification
F-0010-2024official record ID
Oct 18, 2023report date

Recall record at a glance

Official recordF-0010-2024
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmFairfield Gourmet Food Corp d/b/a David's Cookies
Report dateOct 18, 2023
Recall initiation dateSep 13, 2023
Quantity120 cASES
LocationFairfield, NJ, United States

Official product description

Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g), plastic package (i.e.) Clamp shell, 8 package per case, Frozen master case (keep refrigerator Retail pack. LOT # BS23212 (Manufactured on July, 31, 2023).

Why the product was recalled

Fairfield Gourmet Food Corp. d/b/a David s Cookies ,28 Industrial Road, Fairfield NJ 07004has initiated a recall of Markside Ultimate Peanut Butter Chocolate Cake, 7 oz.(198g) plastic package (i.e.) Clamp shell 8 package per case, LOT # BS23212 (Manufactured on July, 31, 2023) because of MISLABELED / UNDECLARED ALLERGENS (Peanuts)

Distribution information

The recall product was distributed to the following states : AL, CA, NV, WA, UT, FL, NM, NC, GA, MO, IL, IN, WI, MN, WY, IN, NE, OK, AR, SC and TN.

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.