State

North Carolina product recalls

72,940 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.

Which agencies issued them

These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4551–4575 of 83201

HighFDA (Devices)·Z-0469-2026·2025-11-19
Impact vessel sealers recalled over residual material that may dislodge
Medline is recalling 58,499 reprocessed LigaSure Impact sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.
Product
Medline Renewal Ligasure Impact Sealer/Divider NanoCoated, Compatible with FT10 Generator 18cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0486-2026·2025-11-19
VATS lobectomy stapler boxes recalled over a malformed cover tube press
Covidien is recalling two units of a VATS lobectomy box containing the Signia Small Diameter Curved Tip Intelligent Reload because internal components may move during firing.
Product
Covidien Signia" Small Diameter Curved Tip Intelligent Reload (45mm Vascular/Thin); BOX LOBECTOMIA VATS 3D; CFN: BOX06170V4;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0456-2026·2025-11-19
Portrait vital signs monitors recalled over batteries losing backup power
GE Healthcare is recalling 5,990 Portrait VSM patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Product
Portrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0490-2026·2025-11-19
Reprocessed ultrasonic shears recalled because they may stick in the on position
Stryker Sustainability Solutions is recalling 22,476 reprocessed HARMONIC FOCUS shears because a manufacturing issue may leave them stuck in the on position, causing continuous activation.
Product
HARMONIC FOCUS Shears + Adaptive Tissue Technology, 9 cm Length REF: HAR9F, Reprocessed Device for Single Use, STERILEEO, RX ONLY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0481-2026·2025-11-19
Oxygen concentrator batteries recalled over a chip that can stop oxygen
Philips Respironics is recalling 56 SimplyGo Mini standard battery kits because a defective chip can make the battery fail, shutting down the concentrator and stopping oxygen delivery.
Product
SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113600
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0475-2026·2025-11-19
Maryland jaw sealers 23 cm recalled over residual material inside the device
Medline is recalling 4,007 reprocessed LigaSure Maryland Jaw sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Product
Medline Renewal LigaSure Maryland Jaw Sealer/Divider Nano Coated, Compatible with FT10 Generator 23 cm FT10 SW Version 4.0.1.15 or lower; Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0457-2026·2025-11-19
Monitor batteries recalled because they can lose the ability to charge
GE Healthcare is recalling 2,857 FLEX-3S2P lithium-ion batteries used with patient monitors because they can lose the capability to hold charge and provide backup power.
Product
BATTERY FLEX-3S2P 10.8V 18650 LI-ION SMBUS used with affected patient monitors Model No 2062895-001 Manufacturer Part Number U80296-1R01, revision S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0489-2026·2025-11-19
Hematology analyzers recalled because saturation flags may not be applied
Abbott Laboratories is recalling 833 Alinity hq Analyzers because a software issue means the system does not visibly flag results when saturation is present, which may give incorrect results.
Product
Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalog Number: 09P68-01 Software Version: 5.0 to 5.10.1 for OUS, 5.7 and 5.10.1 in the US Product Description: Alinity hq Analyzer Component: No
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0465-2026·2025-11-19
DigitalDiagnost C90 systems recalled over ceiling carriages resisting vertical movement
Philips is recalling 223 DigitalDiagnost C90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
DigitalDiagnost C90 (1) High Performance, (2) Flex/Value/Chest/ER; Model Number: (1) 712034, (2) 712035;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0500-2026·2025-11-19
Platelet reactivity tests recalled after an uncleared device was distributed
Accriva Diagnostics is recalling 125 boxes, 3,125 tests, of VerifyNow PRUTest because a device without premarket clearance was incorrectly packaged and distributed.
Product
VerifyNow PRUTest Platelet Reactivity Test REF 85225 UDI-DI code: 10711234150078 The VerifyNow PRUTest is a whole blood test used in the laboratory or point of care setting to measure the level of platelet P2Y12 receptor blockade.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0461-2026·2025-11-19
ProxiDiagnost systems recalled over ceiling carriages that resist vertical movement
Philips is recalling 41 ProxiDiagnost N90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
ProxiDiagnost N90; Model Number: 706110;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0484-2026·2025-11-19
Laboratory cuvette arrays recalled over barcodes the analyser cannot read
Becton Dickinson is recalling 29,760 BD Kiestra Isolate Suspension Cuvette Arrays because formatting errors in the 2D barcodes stop the analyser reading the expiration date.
Product
BD Kiestra" Isolate Suspension Cuvette Array; Catalog No.: 246100;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0464-2026·2025-11-19
DigitalDiagnost 4 systems recalled over ceiling carriages hard to move
Philips is recalling 12 DigitalDiagnost 4 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
DigitalDiagnost 4 (1) High Performance, (2) Flex/Value; Model Number: (1) 712031, (2) 712032;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0462-2026·2025-11-19
CombiDiagnost systems recalled over ceiling carriages that resist vertical movement
Philips is recalling 17 CombiDiagnost R90 systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
CombiDiagnost R90; Model Number: 709031;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0463-2026·2025-11-19
Precision CRF systems recalled over ceiling carriages that are hard to move
Philips is recalling 42 Precision CRF systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
Precision CRF; Model Number: 706400;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0466-2026·2025-11-19
Radiography systems recalled over ceiling carriages that are hard to move
Philips is recalling 284 Radiography 7300 C systems because some ceiling suspension telescopic carriages may be difficult to move vertically.
Product
Radiography 7300 C; Model Number: 712037;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0479-2026·2025-11-19
ACL restoration implants recalled from one lot held in sales stock
Miach Orthopaedics is recalling 167 BEAR Implants from a single lot, in an action the record says was limited to sales force trunk stock.
Product
BEAR Implant (Bridge-Enhanced ACL Restoration); Model/Catalog: 1000;
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25E078000·2025-11-18
Mack Trucks Recalls Certain Vehicles Due to Electronic Control Unit Defect
Mack Trucks is recalling certain vehicles because electrical noise may cause the electronic control unit to malfunction, potentially disabling safety systems like ABS and increasing crash risk.
Product
SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E077000·2025-11-18
Volvo Trucks Recalls Bendix EC80 Electronic Control Units for Software Defect
Volvo Trucks is recalling certain Bendix EC80 Advanced Electronic Control Units due to a software defect that may cause safety systems to fail, increasing crash risk.
Product
SERVICE BRAKES, AIR:ANTILOCK:CONTROL UNIT/MODULE recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V798000·2025-11-18
2024 Kawasaki Ninja ZX-6R Motorcycles Engine Stall Recall
Kawasaki is recalling 2024–2026 Ninja ZX-6R motorcycles because a metal crankshaft bushing may seize, causing engine stall and increasing crash risk. Owners are advised not to ride until dealers re-tighten the bushing free of charge.
Product
KAWASAKI — KAWASAKI NINJA ZX-6R
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V797000·2025-11-17
Hyundai IONIQ 5 front seat belt retractors may not be secured
Hyundai is recalling certain 2025 IONIQ 5 vehicles because the seat belt retractors for the driver and front passenger seats may not be securely fastened.
Product
HYUNDAI — HYUNDAI IONIQ 5
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V792000·2025-11-17
Thor motorhome solar panel adhesive can fail allowing detachment
Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Dazzle, Scope, Rize and Twist RVs because the adhesive securing the solar panels to the roof may fail.
Product
THOR MOTOR COACH — THOR MOTOR COACH TWIST, TELLARO, DAZZLE, RIZE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V795000·2025-11-17
Peterbilt 567 and 589 Trucks Recalled for Brake Air Tank Defect
PACCAR is recalling 2026 Peterbilt 567 and 589 trucks because air tanks have insufficient volume, potentially reducing braking performance.
Product
PETERBILT — PETERBILT 589, 567
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V791000·2025-11-17
Thor motorhome solar panel mounting brackets can loosen or break
Thor Motor Coach is recalling certain 2022-2024 Tellaro, Sequence, Twist, Dazzle and other RVs because the solar panel mounting brackets may loosen or break, allowing the panel to detach.
Product
THOR MOTOR COACH — THOR MOTOR COACH TWIST, TRANQUILITY, DAZZLE, FREEDOM ELITE VAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V794000·2025-11-17
Kia K5 fuel tank can expand and melt against hot exhaust
Kia is recalling certain 2021-2024 K5 vehicles because a damaged check valve can let air into the fuel tank, causing it to expand, contact hot exhaust components and melt.
Product
KIA — KIA K5
Category
Vehicle
Distribution
Distributed nationwide