Skip to main content

Callie's Charleston Biscuits Recall: The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes

United States

CompletedClass I

Company
Callie's Charleston Biscuits
Product
Callie's Charleston Biscuits COUTRY HAM BISCUITS; 18 NET WT…
Recall date
October 4, 2018
Source
FDA

Reason for recall

The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes

  1. - Recall initiated
  2. - Reported by source
Recalled products
Product description UPC Quantity Lot / code information
Callie's Charleston Biscuits COUTRY HAM BISCUITS; 18 NET WT. 18 OZ (510 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM Not published in this source record 12,072/18 oz. packages 050417, 052417, 053017, 071017, 072417, 080117, 081417, 082217, 091417, 092717, 101017, 101117, 102417, 110617, 110817, 111417, 112017, 113017, 120817, 121117, 121417, 121817, 122217, 070219, 071519, 081319, 082619, 090819, 091519, 092619, 092719, 101019, 101619, 102319, 110119, 111119, 111419, 112919, 121319, 122119, 010920, 013020, 020620 & 031920.

Distribution

  • Product was shipped to the following states:AK
  • AL
  • AR
  • AZ
  • CA
  • CO
  • CT
  • DC
  • DE
  • FL
  • GA
  • HI
  • IA
  • ID
  • IL
  • IN
  • KS
  • KY
  • LA
  • MA
  • MD
  • ME
  • MI
  • MO
  • MN
  • MS
  • MT
  • NC
  • ND
  • NE
  • NH
  • NJ
  • NM
  • NV
  • OH
  • OK
  • OR
  • PA
  • RI
  • SC
  • SD
  • TN
  • TX
  • UT
  • VA
  • VT
  • WA
  • WI
  • WV & WY.

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0067-2019
Event ID
81184
Status
Completed
Classification
Class I
Company
Callie's Charleston Biscuits
Product description
Callie's Charleston Biscuits COUTRY HAM BISCUITS; 18 NET WT. 18 OZ (510 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM
Quantity
12,072/18 oz. packages
Reason
The firm was notified by one of their vendors that the ham used in their product may be contaminated with Listeria monocytogenes
Recall initiation date
October 4, 2018
Report date
October 31, 2018
Classification date
Not published in this source record
Termination date
Not terminated as of this source record
Distribution pattern
Product was shipped to the following states:AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MO, MN, MS, MT, NC, ND, NE, NH, NJ, NM, NV, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV & WY.
UPC, lot, and code information
050417, 052417, 053017, 071017, 072417, 080117, 081417, 082217, 091417, 092717, 101017, 101117, 102417, 110617, 110817, 111417, 112017, 113017, 120817, 121117, 121417, 121817, 122217, 070219, 071519, 081319, 082619, 090819, 091519, 092619, 092719, 101019, 101619, 102319, 110119, 111119, 111419, 112919, 121319, 122119, 010920, 013020, 020620 & 031920.
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

Other products recalled under this same event

This recall shares FDA event ID 81184 with 1 other product entry in Public Health Trace.

FDA Recall United States Completed Historical recordClass I

Callie's Charleston Biscuits

Product
Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET…
Published
October 31, 2018
Distribution
Product was shipped to the following sta…

View recall →

Responsible company: Callie's Charleston Biscuits

Other recalls from Callie's Charleston Biscuits

FDA Recall United States Completed Historical recordClass I

Callie's Charleston Biscuits

Product
Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET…
Published
October 31, 2018
Distribution
Product was shipped to the following sta…

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
Alaska 1
Alabama 1
Arkansas 1
Arizona 1
California 1
Colorado 1
Connecticut 1
District of Columbia 1
Delaware 1
Florida 1
Georgia 1
Hawaii 1
Iowa 1
Idaho 1
Illinois 1
Indiana 1
Kansas 1
Kentucky 1
Louisiana 1
Massachusetts 1
Maryland 1
Maine 1
Michigan 1
Missouri 1
Minnesota 1
Mississippi 1
Montana 1
North Carolina 1
North Dakota 1
Nebraska 1
New Hampshire 1
New Jersey 1
New Mexico 1
Nevada 1
Ohio 1
Oklahoma 1
Oregon 1
Pennsylvania 1
Rhode Island 1
South Carolina 1
South Dakota 1
Tennessee 1
Texas 1
Utah 1
Virginia 1
Vermont 1
Washington 1
Wisconsin 1
West Virginia 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 "Completed." 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.