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Recalls affecting South Carolina

Data last updated: September 6, 2026 at 10:21 PM UTC

16,707 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
Wording
Class IHigh risk
FoodRecalled February 4, 2017

Jalapeno Colby Jack Cheese packaged as: (a) AMISH CLASSICS Jalapeno Colby Jack EW Fullmoon, Item 17245, 8 oz., UPC 828653102458(b) AMISH CLASSICS Jalapeno Colby Jack Mini Horn, Item 17209, 6 lbs., No UPC

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-1698-2017
Lot/product code:
Lot Numbers: (a) Best if used by: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 4, 2017

Provolone Cheese Salame packaged as: (a) Sutters Quality Foods Provolone Salame, Item 58814, 6 lbs, no UPC

Potential cross contamination from a of product collected by the State Department of Agriculture which tested positive for Listeria Monocytogenes

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-1707-2017
Lot/product code:
Lot Numbers: (a) Best if Used by: 5/6/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 4, 2017

Colby Jack Cheese packaged as follows: (a) m markets of Meijer(R), NET WT 6 LBS (2.72 kg), Item 18755, UPC 71091718755 (b) Amish classics Colby Jack RW Halfmoon, Item 18244, 8 oz, no UPC (c) Meijer Colby Jack EW Halfmoon Chunk, Item 18758, 8 oz, UPC 713733340588 (d) Amish Classics Colby Jack RW Fullmoon, Item 18241, 8 oz, no UPC (e) Amish Classics Colby Jack EW Fullmoon, Item 18245, 8 oz, 828653182450 (f) Deli Readi Colby Jack 1/2 Moon Slices, Item 18830, 1 lb, UPC 6 34660 62875 7 (g) Amish Classics Colby Jack Mini Horn, Item 18209, 6 lbs, no UPC (h) LIPARI OLD TYME Colby Jack EW Halfmoon, Item 18703, 8 oz, UPC 094776102211 (I) Deli Readi Colby Jack St Pk 1oz Mn Hrn Slice, Item 18831, 2 lbs, UPC 634660628603 (j) Dietz & Watson Colby Jack Mini Horn, Item 18740, 6 lbs, no UPC (k) Winder Farms Colby Jack St Pk .75oz Slice, Item 18790, 1 lb, UPC 828653187905

Sample of product collected by the State Department of Agriculture tested positive for Listeria Monocytogenes

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-1695-2017
Lot/product code:
Lot Numbers: (a) Sell by Date: 02/28/2017 through 08/14/2017 (b) Best if used by: 02/28/2017 through 08/14/2017 (c) Best if used by: 02/28/2017 through 08/14/2017 (d) Best if used by: 02/28/2017 through 08/14/2017 (e) Best if used by: 02/28/2017 through 08/14/2017 (f) USE BY: 02/28/2017 through 08/14/2017 (g) Best if used by: 02/28/2017 through 08/14/2017 (h) Best if used by: 02/28/2017 through 08/14/2017 (i) Best if used by: 02/28/2017 through 08/14/2017 (j) Best if used by: 02/28/2017 through 08/14/2017 (k) Best if used by: 02/28/2017 through 08/14/2017
Recalling firm:
MDS Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 12, 2017

EpiPen Jr. 2-Pak (Epinephrine) Auto-Injectors 0.15 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS: Epipen Auto-Injector Jr. 0.15 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0691-2017
Lot/product code:
US lot 5GN767, expiration April 2017; lot 5GN773, expiration April 2017; lot 6GN215, expiration Sep 2017: INTERNATIONAL lot 5GR765, expiration March 2017; lot 5GK771, expiration April 2017; lot 5ED824, expiration April 2017; and lot 6ED117, expiration ***
Recalling firm:
Meridian Medical Technologies a Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled March 12, 2017

EpiPen 2-Pak (Epinephrine) Auto-Injectors 0.3 mg, Rx only, Manufactured for Mylan Specialty L.P., Morgantown WV 26505 by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company; NDC 49502-500-02 ---- ALSO LABELED OUTSIDE THE US AS ---- Epipen Auto-Injector 0.3 mg -Bright Stock labeled for multiple countries- manufactured for Mylan by Meridian Medical Technologies, Inc., Columbia, MD 21046, a Pfizer company.

Defective Delivery System; reports of the device failing to activate which could result in a patient not receiving medication

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0690-2017
Lot/product code:
US: lot 5GM631, exp. April 2017; lot 5GM640, exp. May 2017; lot 6GM072, exp. Sep 2017; lot 6GM082, exp. Sep 2017; lot 6GM088, exp. Oct 2017; lot 6GM087, exp. Oct 2017; lot 6GM198, exp. Oct 2017; lot 6GM081, exp. Sep 2017; lot 6GM091, exp. Oct 2017; lot 6GM199, exp. Oct 2017: INTERNATIONAL: lot 5FA665, exp. April 2017; lot 5GU763, exp. May 2017; lot 6FA293, exp. Oct 2017; lot 6FA292, exp. Oct 2017; lot 6GH294, exp. Oct 2017.
Recalling firm:
Meridian Medical Technologies a Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled April 21, 2017

Infant 25% DEXTROSE Injection, USP, 2.5 g (250 mg/mL), 10 mL Unit of Use Single-dose Syringe per carton, Rx only, Hospira Inc., Lake Forest, IL 60045, NDC 0409-1775-10

Presence of Particulate Matter: human hair found within an internal sample syringe.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0862-2017
Lot/product code:
Lot 58382EV*, Exp 1OCT 2017, *lot may be followed by 01 or 02
Recalling firm:
Hospira Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled March 6, 2018

Maurice's Honey Southern Gold BBQ Sauce; Net Wt. 18 oz. bottles; UPC Code 0 7561654332 6 and Carolina Gold Honey Sauce; Net Wt. 18 oz. bottle; UPC Code 0 7561654383 8

Not listed on the label soy and wheat ingredients

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0978-2018
Lot/product code:
All lots
Recalling firm:
Piggie Park Enterprises Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 13, 2018

Shell Eggs packaged in quantities and styles of pack (plastic and pulp cartons, flats, and boxes)

Shell eggs have the potential to be contaminated with Salmonella Braenderup.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-1410-2018
Lot/product code:
Plant Number P-1065; LOT CODES with a Julian date ranged from 011 - 102; Numerous UPCs
Recalling firm:
ROSE ACRE FARM
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled April 19, 2018

Happy Harvest Leaf Spinach; Net Wt. 13.5 oz (383g); Ingredients: Spinach, Water, Salt. Distributed by Aldi Inc. Batavia, IL 60510; Product of USA; Manufactured In A Facility That Processes Peanuts and Soy. May Contain Peanuts and Soy. Packaged in a steel 2-piece can.

Canned spinach is being recalled due to the potential to contain boiled peanuts instead of spinach.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-1412-2018
Lot/product code:
Lot Code: SPIN71A23IX Use by January 2021; UPC: 041498131289
Recalling firm:
Mccall Farms Inc
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled August 15, 2018

Montelukast Sodium Tablets 10 mg, 30-count bottle, Rx Only, By: Hetero Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahaboob Nagar - 509 301, India, Manfuactured for: Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, NDC 31722-726-30

Labeling: Label Mix-Up - One lot labeled Montelukast Sodium Tablets 10 mg tablets may contain 90 tablets of Losartan Potassium 50 mg.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-0081-2019
Lot/product code:
Lot #: MON17384, Exp 12/19
Recalling firm:
Hetero Labs Limited Unit V
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 4, 2018

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

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

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0067-2019
Lot/product code:
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.
Recalling firm:
Callie's Charleston Biscuits
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 4, 2018

Callie's Charleston Biscuits COCKTAIL HAM BISCUITS; 24 NET WT. 35 OZ (980 g) Callie's Charleston Biscuits; 1895 Avenue F, Charleston, SC 18405 843 577.1198; CALLIESBISCUITS.COM

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

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0066-2019
Lot/product code:
050417, 060617, 060717, 080117, 091917, 092717, 110617, 120417, 121617, 070619, 080819, 101019, 102319, 110119, 111419, 122119 & 010920.
Recalling firm:
Callie's Charleston Biscuits
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 5, 2018

LADYFINGERS GOURMET TO GO SIGNATURE SHAVED COUNTRY HAM ROLLS; ONE DOZEN PER PACKAGE (15oz - 425 grams); ALLERGEN INFORMATION: CONTAINS WHEAT, PRODUCED IN FACILITY THAT PROCESSES PEANUTS AND TREE NUTS. www.ladyfingersofraleigh.com; 919-828-2270; 627 East Whitaker Mill Rd Raleigh, NC 27608; UPC 8 56149 00509 9.

The firm was notified by their vendor that the product may be contaminated with Listeria monocytogenes.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0065-2019
Lot/product code:
All product on the market.
Recalling firm:
Ladyfingers Catering, LLC
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled February 26, 2019

MONARCH SOUTHERN BARBECUE SAUCE MADE WITH MUSTARD NET 128 FL OZ(1 GAL) 3.78L INGREDIENTS: WATER, HIGH FRUTOSE CORN SRYUP, SUGAR, TOMATO PASTE, DISTILLED AND CIDER VINEGAR, SALT ***DISTRIBUTED BY/DISTRIBUIDO POR US FOODS, INC., ROSEMOUNT, IL 60015 UPC 7 58108 60016 4

Monarch Southern BBQ contains soy and wheat. The firm had labels that properly described the product as Monarch Southern BBQ, but did not have the correct UPC, nutrition panel, ingredient statement or allergen declaration.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-1303-2019
Lot/product code:
Product Item number 06678, Lot numbers18352M, 19015M, 19016M, 19030M, 19043M
Recalling firm:
The CF Sauer Company
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled May 27, 2019

"DEEP***GOLDEN RAISINS***NET WT***198g/7oz***DEEP FOODS, INC. UNION, NJ 07083"

Deep Foods Inc., 1090 Springfield Road, Union, NJ-07083 is initiating a recall of Deep Golden Raisins because of not listed on the label sulfites.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-1981-2019
Lot/product code:
This recall covers 7oz, 14oz, and 28oz sizes with the following UPC codes: 7oz: 011433133432 14oz: 011433133449 28oz: 011433433457
Recalling firm:
Deep Foods Inc
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled September 24, 2019

Chef Pierre ¿ SMALL WHOLE GRAIN BANANA MUFFINS NET WT 12 LB (5.44kg) 4 TRAYS/24/2 oz WHOLE GRAIN BANANA MUFFINS KEEP FROZEN CONTAINS WHEAT, EGGS DISTRIBUTED BY TYSON FOOD SERVICE SPRINGDALE, AR 72765-2020 UPC (01) 1 00 32100 08896 8

The firm was notified from a consumer of foreign material in the product. After examination they discovered that the foreign material was "tree nut".

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0040-2020
Lot/product code:
Product: 08896 CP SMMUF 2OZ WG BNNA 4/24CT Lot Codes: 1700072910:15,1700072910:16, 1700072910:17, 1700072910:18, 1700072910:19, 1700072910:20, 1700072910:21, 1700072910:22, 1700072910:23 & 1700072910:00 expiration 3/12/2020
Recalling firm:
Sara Lee Frozen Bakery
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 3, 2019

fresh AND LOCAL CHICKEN SALAD on Croissant; Manufactured for Coremark; NET WT 6 OZ; UPC 0 67068 13105 3

The firm was notified by their supplier of possible contamination of Listeria monocytogenes in the product.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0085-2020
Lot/product code:
Best By: 9/19/19, 9/24/19, 9/26/19, 10/1/19, 10/3/19 & 10/10/19.
Recalling firm:
Grand Strand Sandwich Company,Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled October 3, 2019

LUNCH BOX SANDWICHES CHICKEN SALAD; NET WT 4.5 oz (127G); MADE BY: GS Sandwich Co. Longs, SC 29568 843-399-2999; UPC 0 67068 12105 4

The firm was notified by their supplier of possible contamination of Listeria monocytogenes in the product.

Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
F-0084-2020
Lot/product code:
Fresh - Sell by: 10/08/19, 10/11/19, 10/15/19, 10/18/19, 10/25/19 & 10/29/19. Frozen - Julian Date 26119
Recalling firm:
Grand Strand Sandwich Company,Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Tasty Drops, Hemp Oil Extract, Spearmint, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29081 1

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1473-2020
Lot/product code:
FG003139, FG003166, FG003191, FG003225, FG003253, FG003263
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Pathway To Wellness, CBD Oil, Premium Hemp Oil Drops, Natural, 1000MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Pathway to Wellness

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1464-2020
Lot/product code:
FG003151
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Herbzeedy, Hemp Oil Full Spectrum, Natural, 500 MG CBD, 1 FL OZ (30 ML) bottles, Distributed by: Herbzeedy, Statesboro, GA

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1462-2020
Lot/product code:
FG003122, FG003123
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Acadia Farms, Serenity, soothing mint, 300 MG Hemp Oil, 1 Fl OZ (30 ML) bottles, Distributed by: Acadia Farms, Rehobeth, Massachusetts

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1469-2020
Lot/product code:
FG003177
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Javan Anti Aging and Wellness Institute, CBD Oil, Full Spectrum Hemp Oil, Spearmint, 300MG CBD, 1 FL. OZ (30 ML) bottles, Dist by: Javan Wellness LLC, 1445 Church St NW Unit 24, Washington, DC 20005

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1463-2020
Lot/product code:
FG003283
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

BC Hemp Co., Full Spectrum Hemp Extract, CBD Oil, Natural, 1000MG CBD, 1 FL. OZ (30 ML) bottles, Distributed by: B.C. Hemp Co., LLC, P.O. Box 156, Eau Claire, MI 49111

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1479-2020
Lot/product code:
FG003318
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Tasty Drops Hemp Oil Extract, Spearmint, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76472 1

Chemical contamination: product contains elevated levels of not listed on the label lead.

ALL 50 STATES
Full report

The most serious kind of recall. Using this product could cause serious health problems or death.

Recall #:
D-1449-2020
Lot/product code:
FG003167
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)