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.

3601–3625 of 83201

ModerateFDA (Devices)·Z-1192-2026·2026-02-04
Maxillofacial and plastics packs recalled over cracking MASTISOL adhesive tubing
Medline is recalling 66 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Product
Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL PACK-LF, Kit SKU DYNJ0660040R; 2) PLASTICS VCH, Kit SKU DYNJ39225K; 3) WT BREAST PACK, Kit SKU DYNJ46620I; 4) ENDO / AUG PACK, Kit SKU DYNJ59250I; 5) KMC PLASTIC/GEN PACK-LF, Kit SKU DYNJ65980J
Category
Medical Device
Distribution
Distributed nationwide
ModerateNHTSA·26V065000·2026-02-04
Ember travel trailer certification labels may list incorrect weight information
Ember is recalling certain 2026 E-Series and Overland Series travel trailers because the Federal Certification Label may list incorrect unloaded vehicle weight and cargo carrying capacity information.
Product
EMBER — EMBER E-SERIES, OVERLAND SERIES
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1187-2026·2026-02-04
Cath lab and loop recovery packs recalled over cracking adhesive tubing
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Product
Medline medical procedure convenience kits labeled as: 1) CATH LAB PACEMAKER PACK-LF, Kit SKU DYNJ64837C; 2) LOOP RECOVERY PACK, Kit SKU DYNJT7034;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1165-2026·2026-02-04
Bone graft recalled over an incorrect expiration date on the label
Cerapedics is recalling 237 units of PearMatrix P-15 Peptide Enhanced Bone Graft, 1.0cc, over an incorrect expiration date.
Product
PearMatrix P-15 Peptide Enhanced Bone Graft Bone Graft, 1.0cc REF: 730-010
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1197-2026·2026-02-04
Gynecology and prostate packs recalled over cracking adhesive tubing
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Product
Medline medical procedure convenience kits labeled as: 1) RR-GYN LAPAROSCOPY PACK-LF, Kit SKU DYNJ0395022O; 2) PELVISCOPY PACK-LF, Kit SKU DYNJ0415776Q; 3) DIVA PACK, Kit SKU DYNJ04811O; 4) DA VINCI PROSTATE/COLPOPEXY, Kit SKU DYNJ44864S; 5) MH ROBOTICS PACK, Kit SKU D
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0300-2026·2026-02-04
Glycopyrrolate oral solution recalled after failing impurity and degradation specifications
Novadoz Pharmaceuticals is recalling three lots of Glycopyrrolate Oral Solution, 1 mg/5 mL, after they failed impurities and degradation specifications.
Product
GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1200-2026·2026-02-04
Spine and hip procedure packs recalled over cracking adhesive tubing
Medline is recalling 117 units of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Product
Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE PACK-LF, Kit SKU DYNJ0275635M; 2) SM-SPINE PACK-LF, Kit SKU DYNJ0395037X; 3) TOTAL HIP PACK, Kit SKU DYNJ04809N; 4) MAIN/LAMINECTOMY PACK-LF, Kit SKU DYNJ0565499AN; 5) SCC/SPOC HAND & FOOT PACK, Ki
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1176-2026·2026-02-04
Alphenix INFX-8000C systems recalled over ceiling suspension screws that loosen
Canon Medical Systems is recalling 172 units of the Alphenix INFX-8000C because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.
Product
Alphenix INFX-8000C, interventional fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1189-2026·2026-02-04
Breast biopsy and dermatology packs recalled over cracking adhesive tubing
Medline is recalling 1,928 total of procedure convenience kits containing MASTISOL liquid adhesive, which was recalled after complaints that the butyrate tubing cracked during actuation.
Product
Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT CDS-LF, Kit SKU CDS984853L; 2) BREAST BIOPSY PACK, Kit SKU DYNJ45641B; 3) DERMATOLOGY PACK, Kit SKU DYNJT3658A.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1177-2026·2026-02-04
Alphenix INFX-8000F systems recalled over ceiling suspension screws that loosen
Canon Medical Systems is recalling 98 units of the Alphenix INFX-8000F because fixing screws of the ceiling movement gear in the ceiling suspended arm may become loose.
Product
Alphenix INFX-8000F, interventional fluoroscopic x-ray system
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1218-2026·2026-02-04
LimFlow Vector devices recalled over an incorrect expiration date
LimFlow, Inc. is recalling 33 units of the LimFlow Vector, model VT-US-23, over an incorrect expiration date.
Product
Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0297-2026·2026-02-04
Mouthwash recalled over missing or illegible lot and expiry coding
Haleon is recalling 84,764 bottles of parodontax Active Gum Health Mouthwash, Mint, over the potential for missing or illegible lot and expiration date coding on the bottles.
Product
PARODONTAX — PARODONTAX (CETYLPYRIDINIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·26V061000·2026-02-03
Ford Recalls 2023-2024 Transit Vehicles Due to Engine Crossmember Defect
Ford is recalling 2023-2024 Transit vehicles because an improperly secured engine crossmember may cause the engine to shift, potentially leading to loss of drive power or brake failure.
Product
FORD — FORD TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V062000·2026-02-03
Ford Recalls 2026 E-Transit Vehicles Due to Battery Fire Risk
Ford is recalling 2026 E-Transit vehicles because missing washers in the high-voltage battery pack may cause electrical arcing, increasing the risk of fire or loss of drive power.
Product
FORD — FORD E-TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V060000·2026-02-02
Pierce Recalls 2025 Vehicles Due to Steering Linkage Arm Bolt Issue
Pierce Manufacturing is recalling 2025 Velocity, Arrow XT, Saber, Impel, and Enforcer vehicles because a steering linkage arm bolt may come loose, risking loss of steering control.
Product
PIERCE — PIERCE ENFORCER, IMPEL, VELOCITY, ARROW XT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26E006000·2026-02-02
Chrysler Recalls Mopar Trailer Tow Modules Due to Brake Light Failures
Chrysler is recalling Mopar trailer tow modules because trailer lights and brakes may fail, increasing crash risk.
Product
ELECTRICAL SYSTEM: INTEGRATED TRAILER BRAKE CONTROL recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V059000·2026-02-02
Trucks and SUVs recalled over a trailer tow module design defect
Chrysler is recalling 456,287 Ram and Jeep vehicles because an improperly designed trailer tow module may leave trailer lights unlit and trailer brakes inoperative.
Product
RAM — RAM, JEEP 5500, 1500, 4500, 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V058000·2026-01-30
Grand Design motorhome front seat bases may be improperly tightened
Grand Design is recalling certain 2025-2026 Lineage motorhomes because the seat base on the driver and front passenger seat may have been improperly tightened. This fails FMVSS 207.
Product
GRAND DESIGN — GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V056000·2026-01-30
BMW and Toyota Supra engine starters may overheat and catch fire
BMW is recalling certain 2021-2024 BMW models and 2021-2023 Toyota Supra vehicles because the engine starter may overheat and catch fire due to wear on an internal component.
Product
BMW — BMW, TOYOTA 430I, Z4, 330I, 530I
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·26V057000·2026-01-30
Grand Design Recalls 2026 Solitude RVs for Fire Risk
Grand Design is recalling 2026 Solitude recreational vehicles because a water tank heating pad may fail, increasing the risk of a fire.
Product
GRAND DESIGN — GRAND DESIGN LINEAGE
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·26219·2026-01-29
Pull string teething toys recalled after fifteen reported choking incidents
About 49,410 AiTuiTui Pull String Teething Toys are being recalled. CPSC is aware of 15 choking incidents and two incidents of children able to bite pieces off the silicone strings.
Product
AiTuiTui Pull String Teething Toys
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·26V051000·2026-01-29
Jeep Grand Cherokee rear coil springs may detach while driving
Chrysler is recalling certain 2021-2023 Jeep Grand Cherokee L and 2022-2023 Grand Cherokee vehicles because the rear coil springs may be incorrectly installed and detach from the vehicle while driving.
Product
JEEP — JEEP GRAND CHEROKEE L, GRAND CHEROKEE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·26V054000·2026-01-29
Honda driver seat cushion frame may not have been tightened properly
Honda is recalling certain 2023 Accord and Accord Hybrid, 2024 HR-V and Pilot, and Acura Integra vehicles because the driver's seat cushion frame may not have been tightened properly.
Product
HONDA — HONDA, ACURA ACCORD HYBRID, INTEGRA, ACCORD, HR-V
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·26224·2026-01-29
Minoxidil hair serum kits recalled over packaging that is not child-resistant
About 7,000 Sefudun 5% Minoxidil Hair Growth Serum Kit are being recalled because the packaging is not child-resistant as required by the Poison Prevention Packaging Act.
Product
NorthStar Hot Water Pressure Washers
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·26220·2026-01-29
Electric bicycle rear wheel bolts recalled over breakage when torqued
About 19,890 rear wheel bolts on 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles are being recalled because the bolts can break when torqued, causing wheel separation.
Product
Rear wheel bolts installed on model year 2026 Trek FX+ 1 and Electra Townie Go! electric bicycles
Category
Consumer Product
Distribution
Distributed nationwide