Class ITerminated in FDA datasetRecall initiated Oct 13, 2022

Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g)

Recalling firm: Hammond's Candies Since 1920 II, LLC

Why it was recalled

Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box creating undeclared peanut allergen.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 11, 2024.

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Compare the exact product and package details with the label you have.

ProductHammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6 91355 89889 5, Manufactured for: Hammond's Candies, 5735 Washington St, Denver, CO 80216. Cookies are packaged in sealed, opaque, white, plastic bag, which is packed inside printed on cardstock box. There are 8 boxes /case. Storage - Ambient.
Package size5 OZ
UPC691355898895

FDA code information

6/29/2023A (code affixed with sticker) Master case label indicated with Lot B (Boxes with inkjet printed code not impacted, master cases labeled Lot A not impacted)

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6 91355 89889 5, Manufactured for: Hammond's Candies, 5735 Washington St, Denver, CO 80216. Cookies are packaged in sealed, opaque, white, plastic bag, which is packed inside printed on cardstock box. There are 8 boxes /case. Storage - Ambient.

Extracted codes and context

TypeCode / valueContext
UPC691355898895Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6 91355 89889 5, Manufactured for: Hammond's Candies, 5735 Washington St, Denver, CO 80216. Cookies are packaged in sealed, opaque, whi

Original FDA recall reason

Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box creating undeclared peanut allergen.

Recall details

Recall number
F-0146-2023
Event ID
91009
FDA status
Terminated
Initiated
Oct 13, 2022
Reported
Nov 16, 2022
Classified
Nov 9, 2022
Terminated
Jan 11, 2024
Quantity
216-496 units (27-62 cases)
Location
Denver, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide: AL, AR, AZ, CA, CO, DC, FL, GA, KS, KY, LA, MA, MD, MI, MO, MS, NC, NJ, NM, NY, OH, PA, SC, TN, TX, UT, VA, WA, WY. One location in Canada

FDA source record · F-0146-2023

Data updated September 16, 2026. View official FDA data ↗

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