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Hammond's Candies Since 1920 II, LLC Recall: Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box creating undeclared peanut allergen.

United States

TerminatedClass I

Company
Hammond's Candies Since 1920 II, LLC
Product
Hammond's Salted Caramel Cookies, NET WT. 5 OZ (142g), UPC 6…
Recall date
October 13, 2022
Terminated
January 11, 2024
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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. Not published in this source record 216-496 units (27-62 cases) 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)

Distribution

  • 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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0146-2023
Event ID
91009
Status
Terminated
Classification
Class I
Company
Hammond's Candies Since 1920 II, LLC
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.
Quantity
216-496 units (27-62 cases)
Reason
Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box creating undeclared peanut allergen.
Recall initiation date
October 13, 2022
Report date
November 16, 2022
Classification date
Not published in this source record
Termination date
January 11, 2024
Distribution pattern
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
UPC, lot, and 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)
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Hammond's Candies Since 1920 II, LLC

Other recalls from Hammond's Candies Since 1920 II, LLC

FDA Recall United States Completed Historical recordClass II

Hammond's Candies Since 1920 II, LLC

Product
Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged…
Published
November 13, 2024
Distribution
Nationwide

View recall →

Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Alabama 1
Arkansas 1
Arizona 1
California 1
Colorado 1
District of Columbia 1
Florida 1
Georgia 1
Kansas 1
Kentucky 1
Louisiana 1
Massachusetts 1
Maryland 1
Michigan 1
Missouri 1
Mississippi 1
North Carolina 1
New Jersey 1
New Mexico 1
New York 1
Ohio 1
Pennsylvania 1
South Carolina 1
Tennessee 1
Texas 1
Utah 1
Virginia 1
Washington 1
Wyoming 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.