State

North Carolina product recalls

73,596 recalls have nationwide distribution and so reach North Carolina. 10,299 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total: 10,299
Critical: 1,484
Severe: 2,901
Most recent: 2026-10-21

Of the 10,299 recalls naming North Carolina we have scored against our rubric, 1,484 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,901 (28%) are Severe.

Which agencies issued them

These figures cover only the 10,299 recalls whose distribution notice names North Carolina specifically. The 73,596 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26626–26650 of 83895

HighFDA (Devices)·Z-2501-2021·2021-09-29
Scorpion Portal Vein Access Set Recalled for Cracking Sheaths
Argon Medical Devices is recalling the Scorpion Portal Vein Access Set due to design changes that have caused the sheaths to crack or break at the tips. The affected product was distributed in the United States.
Product
Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture tool (0.040 Stylet or 17ga Needle) through the parenchyma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2494-2021·2021-09-29
Ad-Tech Medical Cable Recalled Due to Incorrect Product Labels
Ad-Tech Lightweight CABRIO Cables with incorrect labels are being recalled. Mislabeling could cause product misidentification affecting proper use in clinical monitoring applications.
Product
Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0809-2021·2021-09-29
Pfizer recalls Chantix tablets for N-nitroso-varenicline impurity
Pfizer is recalling certain lots of Chantix (varenicline tartrate) 0.5mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit.
Product
CHANTIX — CHANTIX (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2495-2021·2021-09-29
Ad-Tech TECH ATTACH Cable Recalled for Incorrect Label Information
Ad-Tech Medical recalled its Lightweight TECH ATTACH Cable due to incorrect labels on affected units. The cables are designed to connect electrodes to third-party monitors and stimulators.
Product
Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0997-2021·2021-09-29
Sysco Atlanta Diced Roma Tomatoes Recalled for Improper Temperature Storage
Sysco Atlanta is recalling Imperial Fresh diced Roma tomatoes due to improper temperature storage that may have made the product unsafe to consume.
Product
IMPERIAL FRESH TOMATO ROMA DICED 3/8 TRAY 1/5lbs Plastic overwrap tray
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-1000-2021·2021-09-29
Minor's Seafood Base recalled for improper temperature storage
Sysco Atlanta is recalling Minor's Seafood Base No MSG GF shipped between July and August 2021 to Georgia, North Carolina, and Tennessee because the product was not held at an appropriate temperature and may be unsafe to consume.
Product
MINOR'S SEAFOOD BASE NO MSG GF 6/16 OZ (1 lb) 453 G UNITS Plastic container (pint) gluten free DISTRIBUTED BY NESTLE PROFESSIONAL NORTH AMERIC, SOLON, OH 44139
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-1001-2021·2021-09-29
Sunny Creek Sprout Bean Fresh recalled for improper temperature storage
Sysco Atlanta is recalling Sunny Creek Sprout Bean Fresh in 1/5 lb plastic bags due to improper temperature storage that could make the food unsafe to consume.
Product
SUNNY CREEK SPROUT BEAN FRESH 1/5lbs Plastic bag
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0998-2021·2021-09-29
Ken's Steakhouse Asian Sesame Dressing Recalled for Temperature Control
Sysco Atlanta is recalling Ken's Steakhouse Asian Sesame Dressing after the product was not held at appropriate temperatures. The improper storage conditions could make the food unsafe to consume.
Product
KEN'S STEAKHOUSE DRESSING ASIAN SESAME DRESSING 4/1gallon Plastic container Ken's Foods Inc Marlborough, MA 01752 MUST BE REFRIGERATED
Category
Food
Distribution
3 states
ModerateFDA (Drugs)·D-0813-2021·2021-09-29
Sirolimus Tablets Recalled for Failed Impurities and Degradation Specifications
American Health Packaging is recalling Sirolimus 1 mg tablets (Lot #1000789, expiring 10/31/2022) distributed nationwide because they failed impurities and degradation specifications.
Product
SIROLIMUS — SIROLIMUS (SIROLIMUS)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0823-2021·2021-09-29
Drug Recall: Chlorzoxazone Tablets Due to Manufacturing Deviations
Glenmark Pharmaceuticals is recalling 1,800 bottles of Chlorzoxazone Tablets USP 375 mg nationwide due to current Good Manufacturing Practice (CGMP) deviations. The recall was initiated on August 27, 2021.
Product
Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC 68462-724-01 Manufactured by: Glenmark Pharmaceuticals Inc., USA 4147 Goldmine Road Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1003-2021·2021-09-29
TULKOFF Ginger Puree Recalled for Improper Temperature Storage
Sysco Atlanta is recalling TULKOFF Ginger Puree because the product was not held at appropriate temperatures, making it potentially unsafe to consume.
Product
TULKOFF Ginger Puree 6/32oz Tubs UPC 1 00 70607 50015 6 Tulkoff Food Products, Inc. Baltimore, MD 21224 KEEP REFRIGERATED
Category
Food
Distribution
3 states
ModerateFDA (Food)·F-0996-2021·2021-09-29
Sysco Atlanta Sweet Potato Dice Recalled for Improper Temperature Storage
Sysco Atlanta is recalling Imperial Fresh Potato Sweet Dice shipped to GA, NC, and TN due to improper temperature storage that may have rendered the product unsafe to consume.
Product
IMPERIAL FRESH POTATO SWEET DICE 1/2, 4/5lbs Plastic overwrap tray
Category
Food
Distribution
3 states
ModerateFDA (Drugs)·D-0828-2021·2021-09-29
Betadine Povidone-Iodine Solution Swabstick recalled for subpotent drug
Avrio Health L.P. is recalling Betadine Solution Swabstick in single and three-count packages nationwide because the product is subpotent—meaning it contains less active ingredient than specified. Consumers should stop using affected lots and consult their healthcare provider if needed.
Product
BETADINE — BETADINE (POVIDONE-IODINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0808-2021·2021-09-29
Chantix Varenicline Tablets Recalled for Nitroso Impurity
Pfizer is recalling Chantix (varenicline) tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit, a manufacturing deviation.
Product
Chantix (varenicline) tablets 0.5mg/1mg, 56 Tablets, Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Ireland, NDC 00069-0471-03. carton containing one blister pack of 11 0.5 mg tablets and one blister pack containing 42.1 mg tablets.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2496-2021·2021-09-29
Ad-Tech TECH ATTACH Cable Recalled Due to Incorrect Labeling
Ad-Tech Medical Instrument Corporation is recalling TECH ATTACH Cables due to incorrect labeling. The cables connect electrodes to third-party monitors and stimulators.
Product
Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0824-2021·2021-09-29
Chlorzoxazone 750 mg Tablets Recalled Due to CGMP Deviations
Glenmark Pharmaceuticals is recalling Chlorzoxazone 750 mg tablets nationwide due to current good manufacturing practice (CGMP) deviations. The voluntary recall affects 4,752 bottles with five affected lot numbers.
Product
Chlorzoxazone Tablets USP 750 mg 100 Tablets Rx Only NDC 68462-725-01 Manufactured by: Glenmark Pharmaceuticals Inc., USA 4147 Goldmine Road Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0814-2021·2021-09-29
Promethazine Syrup Plain Recall Due to Microbial Contamination
Morton Grove Pharmaceuticals is recalling Promethazine Syrup Plain 6.25 mg/5 mL in 1-pint bottles due to potential microbial contamination in liquid sugar batches used during manufacturing.
Product
Promethazine Syrup Plain, 6.25 mg/5 mL (Promethazine Hydrochloride Syrup, USP), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-608-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0810-2021·2021-09-29
Chantix Varenicline Tablets Recalled for N-Nitroso Impurity
Pfizer is recalling specific lots of Chantix (varenicline) 1 mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit. The affected lots were distributed nationwide.
Product
CHANTIX — CHANTIX (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0807-2021·2021-09-29
Carbamazepine 200mg Tablets Recalled for Failed Dissolution Specifications
The Harvard Drug Group is recalling Carbamazepine 200mg tablets (Lot R01562, expiring 10/2022) distributed in North Carolina because they failed to meet required dissolution specifications, which may affect the drug's effectiveness.
Product
CARBAMAZEPINE — CARBAMAZEPINE (CARBAMAZEPINE)
Category
Drug
Distribution
1 state
ModerateFDA (Drugs)·D-0816-2021·2021-09-29
Valproic Acid Oral Solution recalled for microbial contamination
Morton Grove Pharmaceuticals is recalling Valproic Acid Oral Solution (250 mg/5 mL) due to potential microbial contamination in liquid sugar batches used during manufacturing.
Product
Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-621-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0825-2021·2021-09-29
Zonisamide Capsules Recalled for Manufacturing Deviations
Glenmark Pharmaceuticals is recalling Zonisamide Capsules 50 mg nationwide due to manufacturing deviations. The recall affects approximately 15,936 bottles across multiple lots with expiration dates in May 2022.
Product
ZONISAMIDE — ZONISAMIDE (ZONISAMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0993-2021·2021-09-29
Fleischmann's Compressed Fresh Yeast Recall Due to Temperature Control
Sysco Atlanta is recalling Fleischmann's Yeast Compressed Fresh in 24/1 lb packages because the product was not stored at appropriate temperatures, creating potential food safety risk.
Product
FLEISCHMANN'S YEAST COMPRESSED FRESH ESL 24/1lbs Paper/Foil overwrap
Category
Food
Distribution
3 states
ModerateFDA (Devices)·Z-2486-2021·2021-09-29
Microbiologics SARS-CoV-2 Process Control Pellets Recalled for Product Specification Issue
Microbiologics Inc is recalling 218 units of SARS-CoV-2 process control pellets (catalog HE0062S) used to validate diagnostic tests. The FDA Class II recall involves product composition regarding RNA transcript content.
Product
SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use as an external, non-viable control material to evaluate the performance of nucleic acid tests that detect SARS-CoV-2 virus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1002-2021·2021-09-29
Alfalfa Sprouts Recall Due to Improper Temperature Storage
Sysco Atlanta is recalling Sunny Creek and Bloomsbury Organic Farm alfalfa sprouts sold in Georgia, North Carolina, and Tennessee because the product was not held at appropriate temperatures and may be unsafe to consume.
Product
Alfalfa Sprouts 12/4oz Plastic container, sold under the the brand names of: Sunny Creek UPC 7 38015 77740 1 SUNNY CREEK FARM Tryon, NC 28782 and BLOOMSBURY ORGANIC FARMKEEP REFRIGERATED
Category
Food
Distribution
3 states
ModerateFDA (Drugs)·D-0821-2021·2021-09-29
Glenmark Naproxen Sodium Tablets recalled for CGMP deviations
Glenmark Pharmaceuticals is recalling 9,552 bottles of Naproxen Sodium Tablets USP 275 mg nationwide due to CGMP (current Good Manufacturing Practice) deviations identified at the manufacturing facility.
Product
NAPROXEN SODIUM — NAPROXEN SODIUM (NAPROXEN SODIUM)
Category
Drug
Distribution
Distributed nationwide