The Recall Desk

State

North Carolina product recalls

73,388 recalls have nationwide distribution and so reach North Carolina. 10,296 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total
10,296
Critical
1,486
Severe
2,898
Most recent
2026-10-07

Of the 10,296 recalls naming North Carolina we have scored against our rubric, 1,486 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,898 (28%) are Severe.

Which agencies issued them

These figures cover only the 10,296 recalls whose distribution notice names North Carolina specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21576–21600 of 83684

  • SevereFDA (Food)·F-1661-2022·2022-09-07

    Whey Protein Drink Recalled Nationwide for Potential Bacterial Contamination

    Optimum Nutrition Gold Standard 100% Whey Vanilla is being recalled nationwide due to potential contamination with Cronobacter sakazakii and Clostridium botulinum. Affected product has lot code 2321 with best-by date 08/20/2022.

    Product
    Optimum Nutrition Gold Standard 100% Whey Vanilla 11 fl oz (325mL). UPC 7 48927-06410 0. Shake well. Best when served chilled. Manufactured for Optimum Nutrition, Inc., 3500 Lacey Road, Suite 1200, Downers Grove, IL 60515
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1609-2022·2022-09-07

    Pediatric Nutrition Formula Recalled for Potential Bacterial Contamination

    Kate Farms Pediatric Standard Sole-Source Nutrition Formula is recalled nationwide due to findings of potential Cronobacter sakazakii and Clostridium botulinum contamination.

    Product
    kate farms Pediatric Standard Sole-Source Nutrition Formula. 1.2 cal/mL. 250 ML (8.45 FL OZ) Tetra Pak container UPC 8 51823-00690 4. Sold in 12 count case UPC 00851823006997. Refrigerate after opening. Made for: Kate Farms, Inc., 101 innovation Place, Santa Barbara…
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1649-2022·2022-09-07

    Metalogix Self-Drill Half-Pin Surgical Component Recalled for Tip Breakage

    New Standard Device Inc is recalling Metalogix Self-Drill Half-Pins used in external fixation surgery due to reports of tip breakages occurring during surgical procedures.

    Product
    Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill Half-Pin 5x30x215mm REF 620030 Metalogix Self-Drill Half-Pin 5x40x215mm REF 620040 Metalogix Self-Drill Half-Pin 5x60x215mm REF 620060…
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Food)·F-1679-2022·2022-09-07

    Frozen Lentil Soup Recalled for Undeclared Wheat Allergen

    Yem Foods LLC recalls Priyems Sambar Coconut & Onion Spicy Lentil Soup due to undeclared wheat starch found in asafoetida ingredient. The product affects consumers with wheat allergies distributed across multiple states.

    Product
    Priyems Sambar Coconut & Onion Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 000124, 8 retail units per wholesale case, Frozen
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-1660-2022·2022-09-07

    ARCHITECT STAT Troponin-I Reagent Kit Recalled for Insufficient Blocking Agents

    Abbott is recalling one lot of ARCHITECT STAT Troponin-I Reagent Kits due to insufficient heterophilic blocking agents in the conjugate, which may affect test accuracy.

    Product
    ARCHITECT STAT Troponin-I Reagent Kit, REF 2K41-27
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1682-2022·2022-09-07

    Sweetums Sucrose Solution Recalled for Contamination and Leaking Cups

    Clinical Innovations is recalling Sweetums 24% Sucrose Solution used in NICU settings due to leaking cups and black particulates in the solution. The recall affects 1,773 boxes distributed nationwide.

    Product
    Sweetums 24% Sucrose Solution Preservative Free 15 mL cups VPSU15037288. Each box contains 288 cups. Product is aseptically packaged in 15 mL cups with foil lid. Each cup contains 15 mL of USP purified water, 24% sugar, citric acid (buffer). Cup is latex-free, DEHP-free…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1647-2022·2022-09-07

    Siemens Artis icono X-Ray Systems Recalled for Potential Hardware Failure

    Siemens has recalled Artis icono X-ray imaging systems due to a potential hardware issue affecting a specific lot of X-ray tubes. If the error detection mechanism fails, the system cannot release X-rays until it is shut down.

    Product
    Artis icono biplane- Model No. 11327600 Artis icono floor- Model No. 11327700
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1648-2022·2022-09-07

    Siemens Dimension Vista CA 15-3 Diagnostic Cartridges Recalled for Measurement Bias

    Siemens Healthcare Diagnostics is recalling Dimension Vista CA 15-3 Flex reagent cartridges because the diagnostic test can produce inaccurate results, reading 26–33% lower than actual values, potentially delaying appropriate patient treatment decisions.

    Product
    Dimension Vista LOCI CA 15-3 Flex reagent cartridge. In Vitro Diagnostic for the quantitative measurement of CA 15-3. Siemens Material Number (SMN)/Ref Catalog Number : 10464344/K6456
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2022·2022-09-07

    Eye imaging device software defect affects surgical planning calculations

    Pentacam eye imaging devices with certain software versions have a bug that causes inaccurate surgical planning printouts for toric intraocular lens procedures.

    Product
    Pentacam AXL REF 70100, Pentacam HR REF 70900. Used to image the anterior segment of the eye.
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Devices)·Z-1666-2022·2022-09-07

    Radiographic imaging system may exceed radiation dose limits in biplane mode

    Canon Medical's Alphenix i imaging systems may deliver radiation dose rates exceeding acceptable limits during biplane fluoroscopic procedures. Sixteen systems nationwide with software versions 8.0, 9.0, or 9.2 and TFP 1200C detector are affected.

    Product
    INFX-8000V. For radiographic and fluoroscopic studies and intervention.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22V671000·2022-09-07

    Nissan Titan vehicles recalled for transmission parking pawl failure risk

    Nissan is recalling 2020-2023 Titan vehicles and certain other models because the transmission parking pawl may fail to engage in park, risking vehicle rollaway and crash.

    Product
    NISSAN — NISSAN TITAN, FRONTIER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1652-2022·2022-09-07

    RT-PCR Kit Recalled Due to False Positive Test Results

    Qiagen's FGFR RGQ RT-PCR Kit may produce false positive results, leading to incorrect lab reports. This could expose cancer patients to inappropriate or suboptimal treatment.

    Product
    FGFR RGQ RT-PCR Kit (RUO, not IVD) REF 8747010
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Food)·F-1581-2022·2022-09-07

    Arborio Rice Recalled for Possible Glass Contamination

    Multiple Arborio rice products are being recalled by Woodland Foods LLC due to possible presence of glass pieces. Consumers should not use the affected products.

    Product
    Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice, 25 lbs. bag UPC 00687080069143 Sysco International X06D05 Arborio Rice, 25 lbs. bag in box UPC 00074865718257 DGourmet.com X06C Arborio Rice, 10 lbs. bag in…
    Category
    Food
    Distribution
    23 states
  • HighFDA (Food)·F-1684-2022·2022-09-07

    Clinical Innovations Sweetums Sucrose Solution Vials Recalled for Contamination

    Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to complaints of leaking, black liquid, and black particulates in product vials. The recall affects neonatal products distributed nationwide and internationally.

    Product
    Sweetums 24% sucrose solution preservative free. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1645-2022·2022-09-07

    X-Ray Imaging System X-Ray Tube Hardware Defect Worldwide Recall

    Siemens has recalled Artis Q and Artis Q.zen X-ray imaging systems due to a potential X-ray tube hardware defect. In rare cases, if error detection fails, the system will not be able to release X-ray until shut down; 1,389 units are affected globally.

    Product
    Artis Q floor- Model No. 10848280 Artis Q ceiling- Model No. 10848281 Artis Q biplane- Model No. 10848282 Artis Q zeego- Model No. 10848283 Artis Q.zen floor- Model No. 10848353 Artis Q.zen ceiling- Model No. 10848354 Artis Q.zen biplane- Model No. 10848355
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1681-2022·2022-09-07

    Priyems Mango Pickles recalled for undeclared wheat starch

    Yem Foods LLC is recalling Priyems Mango Pickles (1lb/454g) due to undeclared wheat starch from asafoetida. Consumers with wheat allergies may be at risk.

    Product
    Priyems Mango Pickles 1lb/454g UPC 8 61754 000179, 10 retail units per wholesale case, Refrigerated
    Category
    Food
    Distribution
    15 states
  • HighFDA (Devices)·Z-1651-2022·2022-09-07

    therascreen FGFR RGQ Kit Recalled for Increased False Positive Results

    Qiagen's therascreen FGFR RGQ RT-PCR Kit is being recalled for increased false positive results in 29 distributed kits. False positives could lead to incorrect lab reports and inappropriate cancer treatment for patients.

    Product
    therascreen FGFR RGQ RT-PCR Kit (CE IVD, not sold in the US) REF 874711
    Category
    Medical Device
    Distribution
    4 states
  • HighFDA (Devices)·Z-1672-2022·2022-09-07

    Medical device software error affects toric IOL surgical planning accuracy

    A software defect in the Pentacam AXL Wave eye imaging device's IOL calculator may inaccurately reflect alignment axis and incision position for toric lens surgeries. This affects 21 systems distributed across the U.S.

    Product
    Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Drugs)·D-1468-2022·2022-09-07

    Colgate Anticavity Fluoride Toothpaste Recalled for Improper Storage Conditions

    Family Dollar is recalling Colgate OPTIC WHITE CHARCOAL COOL MINT toothpaste (Net Weight 4.2 oz., UPC 0 35000 97872 1) distributed to stores in 11 states due to improper temperature storage during manufacturing.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL COOL MINT PASTE, Net Wt. 4.2 OZ. UPC 0 35000 97872 1. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1674-2022·2022-09-07

    Pentacam HR Medical Device Software Error Impacts Surgical Planning

    A software error in the Pentacam HR eye imaging device causes inaccurate IOL calculator output for toric intraocular lens surgical planning. Nineteen systems are affected.

    Product
    Pentacam HR REF 70900. Used to image the anterior segment of the eye.
    Category
    Medical Device
    Distribution
    37 states
  • HighNHTSA·22V670000·2022-09-07

    BMW X7 Third-Row Seat Backrest Springs May Not Lock Properly

    BMW is recalling 2019-2022 X7 models with third-row seats because compression springs may not have been properly installed, causing the seat backrest to potentially fail to lock in a crash.

    Product
    BMW — BMW X7
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1563-2022·2022-09-07

    Philips Radiography System Firmware Defect Risks Incorrect Radiation Dose

    Philips DigitalDiagnost C50 1.1 radiography systems contain a firmware defect in the Wallstand VS2 board that may cause incorrect radiation dose and anatomic marker misalignment. Eleven affected systems were distributed nationwide.

    Product
    DigitalDiagnost C50 1.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1685-2022·2022-09-07

    Sucrose solution vials recalled nationwide for contamination and leaking

    Clinical Innovations is recalling Sweetums 24% sucrose solution vials due to reports of leaking containers and contamination with black liquid and particulates. The product is used in hospital settings including neonatal intensive care units.

    Product
    Sweetums 24% sucrose solution with preservative. Vials containing 1ml or 2ml of 24% sucrose in purified water. Product is administered by drop using vials and tip allows controlled administration directly to tongue or buccal surface. Product is only used in the hospital…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1465-2022·2022-09-07

    Colgate OPTIC WHITE PRO Series Toothpaste Recalled for Improper Storage

    Family Dollar Stores is recalling 1,120 packages of Colgate OPTIC WHITE PRO SERIES toothpaste due to improper temperature storage conditions that deviate from cGMP standards.

    Product
    Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES, Stain Prevention, 5% Hydrogen Peroxide, Net Wt. 2.1 OZ. (59 g) UPC 0 35000 99658 9. Dist. by: Colgate-Palmolive Company New York, NY 10022 U.S.A.
    Category
    Drug
    Distribution
    Distributed nationwide