State

North Carolina product recalls

73,566 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: 1,486
Severe: 2,899
Most recent: 2026-10-21

Of the 10,299 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 2,899 (28%) are Severe.

Which agencies issued them

These figures cover only the 10,299 recalls whose distribution notice names North Carolina specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24826–24850 of 83865

HighFDA (Devices)·Z-0619-2022·2022-02-16
GE Healthcare MR superconducting magnets recalled due to cryogen ventilation system defect
GE Healthcare has recalled 17,228 MR superconducting magnets used in nuclear magnetic resonance imaging systems because the cryogen ventilation system does not meet required venting standards. The recall affects devices distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare MR MAX System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V083000·2022-02-16
2021-2022 Ford Mustang Front Passenger Knee Air Bag Weld Defect
Ford is recalling 2021-2022 Mustang vehicles due to insufficient welds on the front passenger knee air bag, which could deploy improperly and increase injury risk during crashes. Affected owners should contact dealers for a free replacement.
Product
FORD — FORD MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0614-2022·2022-02-16
GE SIGNA MRI Systems Recalled for Cryogen Ventilation Defect
GE Healthcare is recalling 17,228 MRI systems with a potential cryogen ventilation system defect that may not meet regulatory venting requirements.
Product
GE Healthcare MR superconducting magnets, a component of GE SIGNA 3.0T with Excite MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V084000·2022-02-16
Audi Recalls 2022 E-Tron GT for Rear Seat Belt Wiring Issue
Audi is recalling 2022 E-Tron GT vehicles because the center seat belt wiring harness may block access to child seat anchors, preventing proper securing.
Product
AUDI — AUDI E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0566-2022·2022-02-16
Avanos MIC Percutaneous Gastrostomy Kit Recalled for Bolster Sizing Defect
Avanos Medical is recalling the MIC Percutaneous Endoscopic Gastrostomy PEG Kit because the external retention bolster may be larger than the tube, creating a risk of improper fit and potential device failure.
Product
MIC* Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors - 20 Fr-PULL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0590-2022·2022-02-16
GE Healthcare MRI Systems Cryogen Ventilation System Defect Recall
GE Healthcare is recalling SIGNA Premier MRI systems due to a cryogen ventilation system that does not meet venting requirements. Approximately 17,228 affected devices were distributed worldwide.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Premier System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0592-2022·2022-02-16
GE Healthcare MRI superconducting magnets recalled for improper cryogen venting
GE Healthcare has recalled SIGNA Pioneer MRI systems due to potential cryogen ventilation defects that do not meet safety requirements. Approximately 17,228 devices are affected nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Pioneer System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22081·2022-02-16
American Landmaster Utility Vehicles Recalled for Steering Shaft Separation
American Landmaster has recalled about 1,050 utility vehicles (EV, L3, L4, L5, L5W, and L7 models) because the steering shaft can separate from its joint, causing loss of control and crash hazards. Seven steering shaft separations have been reported with no injuries yet.
Product
American Landmaster EV, L3, L4, L5, L5W and L7 Utility Vehicles (UTVs)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V086000·2022-02-16
2019 Volkswagen Atlas: Missing GVWR Label on Side-Step Models
Volkswagen is recalling certain 2018-2021 Atlas and Atlas Cross Sport vehicles equipped with side steps due to a missing GVWR label that reflects the additional weight, increasing overloading risk.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0613-2022·2022-02-16
GE MRI superconducting magnet systems recalled for cryogen ventilation system defect
GE Healthcare is recalling 17,228 MR superconducting magnet systems due to a potential cryogen ventilation system that does not meet venting requirements. The defect could pose safety risks to healthcare facilities and their staff.
Product
GE Healthcare MR superconducting magnets, a component of GE 3.0T SIGNA Infinity TwinSpeed with Excite MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0612-2022·2022-02-16
GE Healthcare MRI superconducting magnets recalled for cryogen ventilation defect
GE Healthcare is recalling 17,228 MRI superconducting magnets that may have improper cryogen ventilation systems. The defect could fail to properly vent cryogenic materials in the SIGNA 3.0T MR System.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA 3.0T MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0589-2022·2022-02-16
QC Blood Culture Identification Panel Recall for Incorrect Antibiotic Susceptibility Test Results
Microbiologics recalls KWIK-STIK blood culture identification quality control panels due to incorrect susceptibility test results. High-level Gentamicin Synergy values were out of specification, risking inaccurate diagnostic guidance.
Product
QC Sets and Panels, KWIK-STIK Blood Culture Identification (BCID) Verification Panel (Live Culture). KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0585-2022·2022-02-16
Quality Control Kit for Antibiotic Susceptibility Testing Returning Incorrect Results
Microbiologics Inc is recalling KWIK-STIK quality control kits used by laboratories because certain lots return incorrect test results that could affect laboratory testing accuracy.
Product
KWIK-STIK, Quality control kit for culture media, sold as: a. KWIK-STIK 2-pack Enterococcus faecalis derived from ATCC 51299 b. KWIK-STIK 6-pack Enterococcus faecalis derived from ATCC 51299
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V087000·2022-02-16
Ford F-250 and F-350 Driveshaft Fracture Risk From Loose Insulators
Ford is recalling 2017–2022 F-250 and F-350 Super Duty trucks. Underbody insulators may loosen and damage the aluminum driveshaft, potentially causing loss of drive power or vehicle control.
Product
FORD — FORD F-250 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0615-2022·2022-02-16
GE Healthcare MRI Superconducting Magnet Cryogen Ventilation System Defect
GE Healthcare MR superconducting magnets in SIGNA MRI systems may have cryogen ventilation systems that do not meet safety venting requirements. Approximately 17,228 systems are affected.
Product
GE Healthcare MR superconducting magnets, a component of GE SIGNA Excite 1.5T MR System, GE SIGNA Excite 3.0T MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0631-2022·2022-02-16
Knee Replacement Component Recalled for Adhesive Residue Risk
DePuy Orthopaedics is recalling ATTUNE Revision knee implant components due to possible adhesive residue on the surface. If undetected before surgery, the residue may cause soft tissue irritation or infection.
Product
ATTUNE REVISION POSTERIOR FEMORAL AUGMENT SZ 9 12MM-intended as a Component in total knee arthroplasty (TKA) revision surgeries Product Number: 154909003
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0563-2022·2022-02-16
Arterial Line Kits recalled due to guidewire-needle incompatibility
Argon Medical Devices is recalling Arterial Line Kits because the included guidewires don't fit through the kit's needles. This could cause procedure delays and minor blood loss.
Product
1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0597-2022·2022-02-16
GE Healthcare MRI Magnets Recalled for Inadequate Cryogen Ventilation
GE Healthcare is recalling MRI magnets used in SIGNA MR355 and MR360 systems that could have cryogen ventilation systems not meeting venting requirements. These systems were distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA MR355 and SIGNA MR360 System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·22082·2022-02-16
Viking 5 Series Freestanding Gas Ranges Recalled for Gas Leak and Fire Risk
Viking Range is recalling about 3,050 Viking 5 Series freestanding gas ranges because the rigid gas tubing can separate at burner joints, creating a risk of gas leak and fire. Consumers should stop using the bake, broil, and griddle functions immediately and contact Viking for a free repair.
Product
Viking 5 Series Freestanding Gas Ranges
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0588-2022·2022-02-16
Diagnostic Quality Control Microorganism Set Fails Gentamicin Susceptibility Specifications
Microbiologics Inc is recalling 139 units of KWIK-STIK AST-GP QC microorganism sets due to incorrect susceptibility test results. The products failed gentamicin synergy specifications and could affect the accuracy of laboratory diagnostic testing.
Product
QC Sets and Panels, KWIK-STIK AST-GP (6 Strains) QC Set. KWIK-STIK kit that contains Catalog Number 0959P. In Vitro Diagnostic Control microorganisms
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0583-2022·2022-02-16
LYFO DISK Streptococcus Pneumoniae Culture Kit Recalled for Bacterial Contamination
Microbiologics Inc is recalling LYFO DISK Streptococcus pneumoniae microorganism culture kits (lot 947-126-1) distributed worldwide due to potential contamination with E. coli, Staphylococcus epidermidis, and S. warneri.
Product
LYFO DISK(TM), LYFO DISK(TM) Streptococcus pneumoniae derived from ATCC(R) 49619(TM). LYFO DISK microorganisms are packaged in a resealable vial that contains 6 lyophilized microorganism pellets and a desiccant to prevent adverse moisture accumulation. The LYFO DISK…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0611-2022·2022-02-16
GE Healthcare MRI Systems Recalled for Inadequate Cryogenic Ventilation
GE Healthcare has recalled 17,228 MRI systems because the cryogenic ventilation system does not meet safety requirements. Systems were distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare Brivo MR355 System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0598-2022·2022-02-16
GE Healthcare MRI Systems with Potentially Non-Compliant Cryogen Ventilation Systems
GE Healthcare has recalled approximately 17,228 MRI systems due to cryogen ventilation systems that may not meet required venting standards. The issue affects systems distributed nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA MR380 System, nuclear magnetic resonance system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0617-2022·2022-02-16
GE Healthcare MRI systems recalled for cryogenic ventilation defect
GE Healthcare MRI systems may have cryogenic ventilation systems that do not meet venting requirements. The recall affects 17,228 devices distributed nationwide and globally. Healthcare facilities should contact GE Healthcare for corrective actions.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA Horizon Cx System (sold under SIGNA Horizon Cx, SIGNA Horizon Lx, SIGNA Infinity, SIGNA MR/I, SmartSpeed, EchoSpeed Plus, and HighSpeed Plus), nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0606-2022·2022-02-16
GE Healthcare MRI Systems Recalled for Inadequate Cryogen Ventilation
GE Healthcare SIGNA HFO/I MR Systems may have cryogen ventilation systems that do not meet venting requirements. Approximately 17,228 systems are affected nationwide and internationally.
Product
GE Healthcare MR superconducting magnets, a component of GE Healthcare SIGNA HFO/I MR System, nuclear magnetic resonance imaging system.
Category
Medical Device
Distribution
Distributed nationwide