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Recalls affecting North Carolina

Data last updated: September 6, 2026 at 11:49 PM UTC

17,100 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
Wording
Class IHigh risk
DrugRecalled August 4, 2016

Bupivacaine Hydrochloride Inj., USP (2.5 mg/mL) 0.25%, packaged in 30 mL Single-dose Preservative-Free vials, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-1159-02

Presence of particulate matter: Confirmed customer report for the presence of particulate matter within a single vial.

ALL 50 STATES
Full report

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

Recall #:
D-0218-2017
Lot/product code:
Lot # 59064DK, Exp. 11/17
Recalling firm:
Hospira Inc., A Pfizer Company
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled August 5, 2016

Eastern Feast, Green Raisin, 7 oz, 11 oz, and 14 oz plastic containers.

Initiated by the Florida Department of Agriculture and Consumer Services due to not listed on the label sulfites on the finished product label.

Full report

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

Recall #:
F-0621-2017
Lot/product code:
No lot codes
Recalling firm:
Commerce International 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 May 11, 2017

De Mi Pais, Queso Fresco, Whole Milk Cheese, Net Wt 16 oz.. (1 lb)

Product contaminated with Listeria monocytogenes

Full report

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

Recall #:
F-2409-2017
Lot/product code:
Exp 09/19/2017, UPC 8-96211-00235-9
Recalling firm:
Global Garlic, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled May 11, 2017

Queso Fresco x LB (Barra)/ Whole Milk Cheese, Net Wt 5-6 lbs.

Product contaminated with Listeria monocytogenes

Full report

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

Recall #:
F-2410-2017
Lot/product code:
Exp 06/17/2017, no UPC
Recalling firm:
Global Garlic, 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
FoodRecalled May 18, 2018

Pious Lion Pure Premium Potent White Maeng DA, Bright Uplifting Energy, 4 oz plastic bag. 833-AVL-KRTM www.piouslion.com

The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.

Full report

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

Recall #:
F-1547-2018
Lot/product code:
There are no codes on the product.
Recalling firm:
Pious Lion
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled May 18, 2018

Pious Lion Pure Premium Potent Limited Release Pink Bali, 1 oz plastic bag. 833-AVL-KRTM www.piouslion.com

The firm was notified by the North Carolina Dept. of Agriculture that the product contains Salmonella.

Full report

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

Recall #:
F-1546-2018
Lot/product code:
There are no codes on the product.
Recalling firm:
Pious Lion
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled June 19, 2018

DRY ROASTED PEANUT MEAL NET WT 30LBS Peanut Processors of Sherman Hwy 87 & Albert Street, Dublin, NC 28332

The firm was notified by their customer that the product test positive for Salmonella

Full report

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

Recall #:
F-1653-2018
Lot/product code:
ITEM# 2180 LOT# G-18151 PO# PL3-402521 JULIAN DATE 18151
Recalling firm:
Peanut Processors, Inc.
View official FDA record (opens in a new tab)
Class IHigh risk
FoodRecalled June 19, 2018

DRY ROASTED MEDIUM CHOP PEANUT GRANULES NET WT 30LBS (13.61 KGS) Peanut Processors of Sherman Hwy 87 & Albert Street, Dublin, NC 28332

The firm was notified by their customer that the product test positive for Salmonella

Full report

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

Recall #:
F-1652-2018
Lot/product code:
LOT# G-18151 JULIAN DATE: 18151 & LOT #G-18158 JULIAN DATE 18158
Recalling firm:
Peanut Processors, 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
DrugRecalled June 18, 2020

Tasty Drops Hemp Oil Extract, Berry, 1 FL. OZ (30ML) bottles, 300MG CBD, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76469 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-1448-2020
Lot/product code:
FG003175
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, 1000MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 8 02991 76539 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-1474-2020
Lot/product code:
FG003095
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)
Class IHigh risk
DrugRecalled June 18, 2020

Made by Hemp 1000MG Hemp Extract, French Vanilla, 1 OZ (30 ML) bottles, Dist by: MHR Brands, Jenison, MI, UPC 8 02991 76553 7

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-1451-2020
Lot/product code:
FG003107
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, Berry, 500MG CBD, 1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29083 5

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-1470-2020
Lot/product code:
FG003137, FG003174, FG003197, FG0057
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, Vanilla, 1500MG CBD,1 FL. OZ (30ML) bottles, Dist by: Tasty Hemp Oil, Jenison, MI, UPC 6 96305 29086 6

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-1477-2020
Lot/product code:
FG003144, FG003249
Recalling firm:
MICHIGAN HERBAL REMEDIES
View official FDA record (opens in a new tab)