State
73,213 recalls have nationwide distribution and so reach North Carolina. 10,294 additional recalls listed North Carolina specifically in their distribution scope.
Of the 10,294 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 2,536 (25%) are Severe.
Which agencies issued them
These figures cover only the 10,294 recalls whose distribution notice names North Carolina specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies found in gift basket #925 due to undeclared tree nuts. The product poses a health risk to consumers with tree nut allergies.
Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in gift basket #927 due to undeclared tree nut allergen. The cookies were distributed nationwide.
Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies distributed nationwide in gift baskets due to undeclared tree nuts. Consumers with tree nut allergies face risk of allergic reaction.
BMW is recalling 2024 430i convertibles because a cracked cylinder head cover may leak oil, increasing the risk of a fire near hot engine components.
Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in #067 Believe Cookie gift baskets (lot codes LC605975 and #106052023) due to undeclared tree nuts. Class I FDA recall; approximately 4,875 cookies nationwide.
Houdini Inc. is recalling Acorn Raspberry Creme Filled Cookies in gift baskets due to undeclared tree nuts allergen. Consumers with tree nut allergies should not consume these products.
Integra LifeSciences is recalling CereLink ICP Extension Cables due to a design defect causing out of range readings. The Class I recall affects 4,941 units distributed nationwide and internationally.
Houdini Inc. is recalling 4,875 Acorn Raspberry Creme Filled Cookies from gift baskets due to undeclared tree nut allergen. These products were distributed across all U.S. states.
Ortho-Clinical Diagnostics is recalling the VITROS 3600 Immunodiagnostic System due to software issues causing system freezes and delayed test result reporting. The delays could affect patient care when rapid results are critical.
Meridian Bioscience is recalling Para-Pak Zn-PVA stool specimen collection vials due to a manufacturing defect that may cause leakage and risk exposure to biological hazards.
Medline Industries is recalling 700 units of Sterile PVP solution because the labeling claims sterility but the contents are non-sterile. The affected products were distributed nationwide in eight states.
Meridian Bioscience is recalling Para-Pak Clean Vials used for stool specimen collection due to a manufacturing defect that increases leakage risk and may expose users to biological hazards.
Toyota is recalling 2022-2023 Corolla Cross vehicles where instrument panel defects may prevent the front-passenger air bag from deploying in a crash. Dealers will replace the panel at no cost.
Medline Industries is recalling sterile prep sticks (REF DYNDA1134) labeled as sterile that contain non-sterile solution, posing infection risk in medical procedures.
Sheetz M.T.go! Double Dipped Chocolatey Peanut Butter Peanuts Snax Mix is being recalled because it contains undeclared soy. The product was distributed in North Carolina, Virginia, and West Virginia.
Toyota and Lexus are recalling certain 2020-2022 vehicles with a faulty Occupant Classification System sensor that may prevent the front passenger air bag from deploying in a crash, increasing injury risk.
The ARTIS icono fluoroscopic x-ray system may falsely detect collisions for up to 30 minutes after startup, requiring manual override with reduced safety protection and limiting diagnostic use.
Change Healthcare's Stratus Imaging PACS software can incorrectly associate patient imaging studies with the wrong patients. Approximately 454 affected units have been distributed nationwide.
Medline Industries recalls 300 units of Sterile Povidone (REF DYNDA2061) after discovering the solution inside foil sachets is non-sterile despite sterile labeling. Affected lots are distributed across eight states.
Audi is recalling 2019-2022 E-Tron vehicles because high-voltage battery modules may overheat and increase fire risk. Dealers will install diagnostic software and replace affected modules at no cost.
Medline PVP Solution (REF DYNDA1858) is being recalled because it is labeled as sterile but contains non-sterile contents. 1,950 units are affected.
GE HealthCare Definium Tempo and Tempo Pro X-ray systems may have been assembled with incorrect bolt torque, creating a risk that Overhead Tube Suspension components could fall.
The Sensica Urine Output System (SCCS1002) displays incorrect timestamps and monitoring data when connected to WiFi or internet due to a time synchronization issue. This malfunction affects the accuracy of patient monitoring records.
The VITROS 5600 laboratory analyzer is being recalled due to software issues causing screen freezes and printer disconnections that delay test result reporting, potentially affecting patient care.
BioReference Health is recalling the 4Kscore Test, a prostate cancer risk diagnostic test used nationwide. The recall follows mathematical modeling performed on over 3,000 specimens regarding digital rectal exam (DRE) information requirements.