The Recall Desk

State

North Carolina product recalls

72,907 recalls have nationwide distribution and so reach North Carolina. 10,261 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total
10,261
Critical
1,476
Severe
2,520
Most recent
2026-09-09

Of the 10,261 recalls naming North Carolina we have scored against our rubric, 1,476 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,520 (25%) are Severe.

These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1051–1075 of 83168

  • SevereFDA (Food)·H-1117-2026·2026-07-01

    Utz Quality Foods Dirty Sour Cream Onion Potato Chips Salmonella Recall

    Utz Quality Foods is recalling 2.0 oz bags of Dirty Sour Cream and Onion Potato Chips due to potential Salmonella contamination. The product was distributed across 32 US states.

    Product
    2.0 oz Dirty Sour Cream and Onion Potato Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Food)·H-1113-2026·2026-07-01

    Zapp's Brand Bayou Blackened Ranch Potato Chips Recalled for Salmonella

    Utz Quality Foods is recalling Zapp's Brand Bayou Blackened Ranch Potato Chips in 2.5oz and 8oz bags due to potential Salmonella contamination. Affected products were distributed across 32 states.

    Product
    2.5oz , 8oz , Zapp's Brand Bayou Blackened Ranch Potato Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Devices)·Z-2587-2026·2026-07-01

    Medline Convenience Kits with Syringes Recalled for Unapproved Design Changes

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CRANIOTOMY PACK-LF DYNJ0101292F DYNJ0101292G HYBRID PACK DYNJ65925A LAMINECTOMY DYNJ905156L DYNJ905156M DYNJ905156N DYNJ905156O DYNJ905156P MAJOR EXTREMITY DYNJ905
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1106-2026·2026-07-01

    Spring & Mulberry Blood Orange Date-Sweetened Chocolate recalled for Salmonella

    Spring & Mulberry Inc. is recalling Blood Orange Date-Sweetened Chocolate bars due to potential Salmonella contamination. Affected products were distributed nationwide.

    Product
    Spring & Mulberry Blood Orange Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470200, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold in
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2585-2026·2026-07-01

    Medline 10mL Polycarbonate Syringes in Medical Procedure Kits Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance. The recall affects 113,843 kits distributed nationwide and in Barbados.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. AAA DYNJ905651B ARTERIOGRAM TRAY 00-402001S AV SHUNT PACK-LF DYNJ0842516F BASIC IR PACK-LF PHS463660F CATH PROCEDURAL TRAY DYNJ43580C CONGENITAL ADD-ON KIT DYN
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2525-2026·2026-07-01

    VOCSN+Pro Respiratory System Backup Battery Alarm Failure Recall

    Ventec Life Systems is recalling VOCSN+Pro respiratory systems due to a damaged backup battery that may prevent the backup alarm from activating during power loss, delaying caregiver awareness of a hazardous condition.

    Product
    VOCSN+Pro package, REF: PRT-00853-000; VOCSN+Pro unit, REF: PRT-00490-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2593-2026·2026-07-01

    Medline convenience kits recalled for unapproved syringe design changes

    Medline Industries recalls convenience kits containing 10mL polycarbonate colored syringes because design changes were made outside of FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. ABDOMINAL VASCULAR-LF DYNJ905291B DYNJ905291C ARTERIOGRAM DYNJ28082G CVICU HEART BAG DYKM2130A ENDOVASCULAR PACK DYNJ0678934J EP PACK DYNJ23456J GENERAL ENDO PA
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0624-2026·2026-07-01

    ChloraPrep One-Step Topical Antiseptic Recalled for Non-Sterility

    CareFusion 213, LLC is recalling ChloraPrep One-Step (chlorhexidine gluconate and isopropyl alcohol) topical applicators due to non-sterility caused by the presence of Aspergillus penicillioides fungal contamination.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2590-2026·2026-07-01

    Medical Device Convenience Kits with 10mL Polycarbonate Syringes Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside FDA-cleared specifications. The recall affects approximately 113,843 kits distributed nationwide.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. CATARACT FULL BODY DYNJ85743 MAJOR VASCULAR PACK DYNJ81610C MINIMALLY INVASIVE PACK-LF DYNJ0843063L PEDIATRIC CATH ANGIO PACK DYNJ54755J PERIPHERAL ARTERIOGRAM RAD DY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1123-2026·2026-07-01

    Sunflower Seeds Recalled for Undeclared Cashew Allergen

    George J Howe Company, Inc. is recalling 25-pound cases of sunflower seeds due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across multiple states.

    Product
    25# Sunflower Seeds C/S
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·H-1098-2026·2026-07-01

    Spring & Mulberry Earl Grey Date-Sweetened Chocolate Bars Recalled

    Spring & Mulberry Inc. is recalling Earl Grey Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.

    Product
    Spring & Mulberry Earl Grey Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a purple box, UPC 850055470231, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indivi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1112-2026·2026-07-01

    Zapp's Bayou Blackened Ranch Kettle Chips Recalled for Salmonella

    Utz Quality Foods, LLC is recalling 1.5oz bags of Zapp's Bayou Blackened Ranch Kettle Chips due to the potential presence of Salmonella. The product was distributed across 32 states.

    Product
    1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
    Category
    Food
    Distribution
    34 states
  • SevereFDA (Drugs)·D-0625-2026·2026-07-01

    ChloraPrep One-Step Antiseptic Solution Recall Due to Sterility Concerns

    CareFusion is recalling 178,000 ChloraPrep One-Step antiseptic applicators (Lot #4073005) nationwide due to potential non-sterility from fungal contamination and seal breaches from paper lidding wrinkles.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2454-2026·2026-07-01

    Medline Convenience Kits with Central Line Insertion recalled for quality issues

    Medline Industries is recalling two models of Convenience Kits (ACC011142 and DYNJ8407) distributed nationwide. The kits contain injectable anesthetics that were recalled due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) DRAWER 6 CENTRAL LINE INSERTIO, Model Number: ACC011142; 2) CENTRAL AND ARTERIAL LINE TOTE, Model Number: DYNJ8407
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2600-2026·2026-07-01

    Abiomed Impella CP Introducer Kit Recalled for Thrombus Risk

    Abiomed is recalling the 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP due to potential thrombus formation during prolonged use. The recall affects 17 units distributed in the United States and Japan.

    Product
    Abiomed 14 Fr x 25 cm Low Profile Introducer Kit for Impella CP. Impella Set Product Code: 1000435. Introducer Product Code: 1000435.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2453-2026·2026-07-01

    Medline Convenience Kits with Lidocaine and Bupivacaine Injections Recalled

    Medline Industries is recalling 22 models of Convenience Kits that contain Lidocaine Hydrochloride Injection and Bupivacaine Hydrochloride in Dextrose Injection due to quality issues found during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) OPEN HEART CDS, Model Number: CDS840144Q; 2) OPEN HEART, Model Number: CDS840150W; 3) OPEN HEART ADULT, Model Number: CDS840396AA; 4) CABG A CDS, Model Number: CDS982269N; 5) OPEN HEART ANESTHESIA PACK, Model Number: CDS983849G; 6) OPEN HE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1119-2026·2026-07-01

    Sunflower Seeds Recalled for Undeclared Cashew Allergen

    George J Howe Company is recalling 6/11oz No Salt Sunflower Seeds due to the presence of undeclared cashew, a tree nut allergen. The product was distributed across 24 U.S. states.

    Product
    6/11oz No Salt Sunflower Seeds
    Category
    Food
    Distribution
    25 states
  • SevereFDA (Food)·H-1105-2026·2026-07-01

    Spring & Mulberry Coffee Date-Sweetened Chocolate bars recalled for Salmonella

    Spring & Mulberry Inc. is recalling Spring & Mulberry Coffee Date-Sweetened Chocolate bars due to potential Salmonella contamination. The affected product was distributed nationwide.

    Product
    Spring & Mulberry Coffee Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light brown box, UPC 850055470224, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1100-2026·2026-07-01

    Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars recalled

    Spring & Mulberry Inc. is recalling Spring & Mulberry Mango Chili Date-Sweetened Chocolate bars nationwide due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it.

    Product
    Spring & Mulberry Mango Chili Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in an orange box, UPC 850055470033, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold indi
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2455-2026·2026-07-01

    Medline Convenience Kits Medical Devices Recalled for Quality Issues

    Medline Industries is recalling four models of Convenience Kits containing Lidocaine and Bupivacaine injections due to quality issues identified during an FDA inspection of the supplier.

    Product
    Medline Convenience Kits: 1) DRAWER 6A ADULT CENTRAL LINE, Model Number: ACC010890; 2) OPEN HEART A OVERHEAD, Model Number: DYNJ910066; 3) OPEN HEART, Model Number: DYNJ9855016V; 4) OPEN HEART, Model Number: DYNJ9855016X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1104-2026·2026-07-01

    Spring & Mulberry Sea Salt Date-Sweetened Chocolate recalled for Salmonella

    Spring & Mulberry Inc. is recalling Sea Salt Date-Sweetened Chocolate bars due to potential Salmonella contamination. Approximately 9,932 individual bars distributed nationwide are affected.

    Product
    Spring & Mulberry Sea Salt Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a grey box, UPC 850055470071, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold individua
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·H-1099-2026·2026-07-01

    Spring & Mulberry Lavender Rose Chocolate Recalled for Salmonella

    Spring & Mulberry Inc. is recalling Spring & Mulberry Lavender Rose Date-Sweetened Chocolate bars due to potential Salmonella contamination. The recall affects multiple batch lots distributed nationwide.

    Product
    Spring & Mulberry Lavender Rose Date-Sweetened Chocolate, Net Wt. 2.1 oz. (60g), individually packaged in a light blue box, UPC 850055470019, Dist. By Spring & Mulberry Raleigh, NC 27606. Wholesale product packed 48 bars (caddied)/56 bars (uncaddied) per case. Retail product sold
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2558-2026·2026-07-01

    Surgify Halo 4.0mm Extendable Surgical Burr Recall for Breakage Risk

    Surgify Medical is recalling Surgify Halo 4.0 mm Extendable surgical burrs due to potential breakage during bi-portal endoscopic spinal surgery. The breakage could create a safety hazard during the procedure.

    Product
    Surgify Halo, 4.0 mm, Extendable, Model/Catalog Number: 40.000.SEE.H1; drills, burrs, trephines & accessories (simple, powered)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2601-2026·2026-07-01

    Abiomed Impella CP Set with SmartAssist 10th Generation Introducer Kits Recalled

    Abiomed is recalling certain Impella CP Set with SmartAssist (10th Generation) units with affected 14Fr Low Profile Introducer Kits due to potential for thrombus (blood clot) formation during prolonged use.

    Product
    Abiomed Impella CP Set with SmartAssist (10th Generation) containing affected 14Fr Low Profile Introducer Kits. Product Codes: 1000413, 1000834.
    Category
    Medical Device
    Distribution
    Distributed nationwide