State

North Carolina product recalls

72,986 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 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7526–7550 of 83247

HighFDA (Devices)·Z-1481-2025·2025-04-09
Nasopore Nasal Dressings Recalled Due to Breached Sterility Seals
Stryker Corporation is recalling Nasopore nasal dressings due to potential breaches in packaging sterility seals that could compromise product sterilization. Approximately 182,344 units have been distributed nationwide.
Product
Nasopore 4cm Standard 2PK fragmentable nasal dressing, Catalog Number 5400-212-004S and Nasopore 4cm Firm 2PK Catalog Number 5400-222-004S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0682-2025·2025-04-09
Lean Cuisine Butternut Squash Ravioli Recalled for Potential Foreign Material
Nestle-USA recalls Lean Cuisine Butternut Squash Ravioli for potential wood-like foreign material. Approximately 50,611 cases distributed across 36 states are affected.
Product
Lean Cuisine Butternut Squash Ravioli, NET WT 9 7/8 OZ (280g), in a plastic tray with film seal, packaged inside a paperboard carton; packed 12 consumer units per case
Category
Food
Distribution
37 states
HighFDA (Devices)·Z-1509-2025·2025-04-09
BD Connecta Stopcocks Recalled for Non-U.S. Instructions Shipped to U.S. Market
BD Connecta Luer-Lok 360 stopcocks were distributed with non-U.S. instructions for use. Healthcare facilities should verify they have the correct U.S. instructions before using affected lot numbers.
Product
BD Connecta BD Luer-Lok 360, REF 394910 UDI-DI code: 00382903949106 Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.
Category
Medical Device
Distribution
35 states
HighFDA (Drugs)·D-0308-2025·2025-04-09
Prescription Duloxetine Capsules Recalled for Nitrosamine Impurity
Breckenridge Pharmaceutical is recalling Duloxetine 30 mg capsules distributed nationwide due to a nitrosamine impurity above acceptable limits. Consumers should consult their doctor about their medication.
Product
DULOXETINE — DULOXETINE (DULOXETINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1472-2025·2025-04-09
Otopore Cylinder Wound Dressing Recalled for Potential Sterility Seal Defect
Stryker Corporation recalls Otopore Cylinder outer ear wound dressing due to potential bubbles in blister seals that may breach the sterile barrier. Affected units were distributed nationwide.
Product
Otopore Cylinder outer ear wound dressing, Firm Catalog Number 5400-020-000 and Forte Catalog Number 5400-020-000TL
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25E025000·2025-04-09
Hiab Recalls Waltco ZS-MK2 Lift Gates Due to Pin Seizure Risk
Hiab USA Inc. is recalling specific Waltco ZS-MK2 series lift gates because insufficient lubrication may cause the cylinder pin to seize, leading to lift gate failure and injury risk.
Product
STRUCTURE:BODY:HATCHBACK/LIFTGATE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1501-2025·2025-04-09
Phoroptor VRx Digital Refraction System Recalled for Detachable Head
Reichert is recalling 1,876 units of the Phoroptor VRx Digital Refraction System (Model 16242) due to an assembly defect that could cause the refraction head to detach during eye examinations.
Product
Phoroptor VRx Digital Refraction System Model Numbers: 16242
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1473-2025·2025-04-09
Stryker Nasopore Nasal Dressing Recalled for Compromised Sterility Seals
Stryker's Nasopore 8cm nasal dressing is being recalled because packaging seals may have bubbles indicating the sterility barrier has been breached. The recall affects 182,344 units distributed nationwide.
Product
Nasopore 8cm fragmentable nasal dressing, Firm Catalog Number 5400-020-008 and Forte Catalog Number 5400-020-008ITL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1500-2025·2025-04-09
Phoroptor VRx Digital Refraction System head may become loose or detach
Reichert, Inc. is recalling 122 units of the Phoroptor VRx Digital Refraction System Model 16241 due to an assembly defect that could cause the device head to become loose and potentially detach.
Product
Phoroptor VRx Digital Refraction System Model Numbers: 16241
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1477-2025·2025-04-09
Hemopore nasal wound dressing packaging seal defect may compromise sterility
Stryker Corporation is recalling 182,344 units of Hemopore nasal/sinus wound dressing due to potential packaging seal defects that could compromise sterility. A bubble on the blister seal may indicate the sterile barrier has been breached.
Product
Hemopore 8cm nasal/sinus temporary wound dressing, Catalog Numbers 5400-020-208 and 5400-020-208ITL (OUS)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1482-2025·2025-04-09
Stryker nasal wound dressing recalled for defective sterile packaging seal
Stryker Corporation is recalling 182,344 units of Hemopore 2PK nasal/sinus wound dressing due to potential bubbles in blister seals that indicate sterility breach. Affected lot numbers are 2024020221, 2024051720, and 2024082321.
Product
Hemopore 2PK nasal/sinus temporary wound dressing, Catalog Number 5400-222-208S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1515-2025·2025-04-09
Ethicon PROLENE BLU Surgical Sutures Recalled for Manufacturing Defect
Ethicon is recalling specific lots of PROLENE BLU surgical sutures due to silicone curing issues during needle manufacturing.
Product
PROLENE BLU 18IN(45CM) USP6-0(M0.7) S/A P-1 PRM
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1514-2025·2025-04-09
Ethicon Surgical Sutures Recalled Due to Silicone Curing Manufacturing Defect
Ethicon Endo Surgery recalls approximately 1,080 surgical sutures due to silicone curing issues identified during manufacturing. The defect may affect suture performance during surgical use.
Product
PDSII¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0306-2025·2025-04-09
Biocon Pharma atorvastatin calcium tablets recalled for failed dissolution specifications
Biocon Pharma is recalling 2,184 bottles of Atorvastatin Calcium Tablets USP 40 mg nationwide. The product failed to meet required dissolution specifications, which may affect medication absorption.
Product
ATORVASTATIN CALCIUM — ATORVASTATIN CALCIUM (ATORVASTATIN CALCIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1517-2025·2025-04-09
Clinical Chemistry Analyzer Recalled for Software Defect in Test Result Calculation
Beckman Coulter is recalling certain DxC 500 AU Clinical Chemistry Analyzers due to a software defect that prevents calculated test results from being recalculated when constituent tests are rerun, potentially delaying patient result reporting.
Product
DxC 500 AU Clinical Chemistry Analyzer, Catalog Numbers/UDI codes: C63519 / 14987666545058 C63520 / 14987666545065 The Beckman Coulter DxC 500 AU Clinical Chemistry Analyzer is an automated chemistry analyzer that measures analytes in samples, in combination with appropriate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1474-2025·2025-04-09
Nasopore nasal dressing recall: compromised sterile barrier seals
Stryker recalls Nasopore 4cm fragmentable nasal dressings due to potential blister seal damage that compromises the sterile barrier. Nationwide distribution affected.
Product
Nasopore 4cm fragmentable nasal dressing, Firm Catalog Number 5400-020-004 and Forte Catalog Number 5400-020-004ITL
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0309-2025·2025-04-09
Prescription Antipsychotic Drug Recalled for Manufacturing Impurity
Glenmark Pharmaceuticals is recalling Chlorpromazine Hydrochloride Tablets due to a manufacturing quality deviation involving an impurity above recommended limits.
Product
CHLORPROMAZINE HYDROCHLORIDE — CHLORPROMAZINE HYDROCHLORIDE (CHLORPROMAZINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0304-2025·2025-04-09
Tolterodine Tartrate Extended-Release Capsules Recalled for Failed Dissolution
Tolterodine Tartrate Extended-Release Capsules, 2 mg (Lot T05393) are being recalled because they failed dissolution specifications. The capsules may not dissolve as intended.
Product
Tolterodine Tartrate Extended-Release Capsules, 2 mg, 30 Capsules (3 x 10) Unit Dose carton, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA, NDC 0904-6592-04.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0307-2025·2025-04-09
Voriconazole Tablets Recalled Due to Manufacturing Practice Deviations
Amerisource Health Services is recalling Voriconazole 50 mg tablets distributed nationwide due to current Good Manufacturing Practice deviations related to repackaging.
Product
VORICONAZOLE — VORICONAZOLE (VORICONAZOLE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1513-2025·2025-04-09
Surgical Suture Needles Recalled Due to Manufacturing Defect
Ethicon Endo Surgery recalls PDS PLUS VIO surgical sutures with needles due to silicone curing defects during manufacturing. 792 units were distributed worldwide.
Product
PDS¿PLUS¿VIO¿30IN(75CM)¿USP6-0(M0.7)¿D/A¿C-1¿MP
Category
Medical Device
Distribution
Distributed nationwide
ModerateNHTSA·25V218000·2025-04-09
Alliance RV Avenue placards may show incorrect weight and capacity figures
Alliance RV is recalling certain 2025 Avenue 23ML travel trailers because the Federal Placard may show incorrect unloaded vehicle weight and cargo carrying capacity.
Product
ALLIANCE RV — ALLIANCE RV AVENUE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V219000·2025-04-08
White River Marine Recalls 2024-2025 Trailstar Boat Trailers Due to Winch Strap Defect
White River Marine Group is recalling 2024-2025 Trailstar TRL and Topper boat trailers because the winch strap may fray and break, allowing the boat to detach.
Product
TRAILSTAR — TRAILSTAR TOPPER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V222000·2025-04-08
Micro Bird Recalls 2023 G5 Transit Buses for Suspension Bolt Defect
Micro Bird is recalling 2023 G5 transit buses because u-bolts securing the suspension may break, increasing crash risk.
Product
MICRO BIRD — MICRO BIRD G5 TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V223000·2025-04-08
Micro Bird Recalls 2023-2024 G5 School Buses for Suspension Bolt Defect
Micro Bird is recalling 2023-2024 G5 school buses because u-bolts securing the suspension may break, increasing crash risk.
Product
MICRO BIRD — MICRO BIRD G5 SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25E024000·2025-04-08
ILJIN Hysolus Recalls Compressed Natural Gas Tanks Due to Rupture Risk
ILJIN Hysolus is recalling specific CNG tanks because the pressure relief device may not fully vent, potentially causing the tank to rupture and increasing the risk of fire and injury.
Product
FUEL SYSTEM, OTHER:STORAGE:TANK ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide