State

North Carolina product recalls

72,907 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 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1376–1400 of 83168

HighFDA (Devices)·Z-2322-2026·2026-06-17
TDC VELOCE 23 gauge vitrectomy cutters may have loose outer knife
TDC VELOCE 23G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.
Product
TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2346-2026·2026-06-17
MIC Safety 24 Fr pull PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 24 Fr PULL, catalog number 7180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 1,006 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PULL Model/Catalog Number: 7180-24
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2313-2026·2026-06-17
Plum Duo Precision IV pumps may not display soft limit alerts
Plum Duo Precision IV Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Product
Plum Duo Precision IV Pump, 40002-0403
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2312-2026·2026-06-17
Plum Duo infusion pumps may not display soft limit alerts
Plum Duo Infusion Pumps are being recalled because under certain conditions the pump may not display a soft limit alert before delivery starts, potentially leading to under- or over-delivery.
Product
Plum Duo Infusion Pump, 40002-0401
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2325-2026·2026-06-17
CGuard Prime 8mm by 30mm carotid stents may fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 30 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx30mm Model/Catalog Number: CND0830
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2362-2026·2026-06-17
EXENT Analyser marked plates as passed without performing quality control
An EXENT Analyser is being recalled after plates 2 and 3 were marked as passed although quality control appeared not to have been performed, despite samples being measured.
Product
Brand Name: EXENT Analyser Product Name: EXENT Analyser Model/Catalog Number: IE800.A Software Version: 1.0.20 Product Description: The EXENT Analyser is an automated analyser intended for the qualitative and quantitative in vitro measurement of analytes in human body fluids
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2406-2026·2026-06-17
MOSAIQ oncology software may fail to load adapted treatment plan
The MOSAIQ Oncology Information System is being recalled because the software may fail to load an adapted baseline shift plan during treatment delivery when a communication error occurs.
Product
MOSAIQ Oncology Information System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2408-2026·2026-06-17
Halyard towel six packs shipped without validated sterilization in Iowa
Halyard Towel Six Packs, kit code AMTS70-01, are being recalled because sealed pouches that had not undergone validated sterilization were inadvertently distributed. 224 kits affected.
Product
Halyard, Towel Six Pack. Kit Code: AMTS70-01.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0586-2026·2026-06-17
Zep alcohol sanitizer spray drums recalled for microbial contamination
Zep Alcohol Sanitizer Spray, ethanol 70%, in 55-gallon drums is being recalled for microbial contamination. Five drums are affected.
Product
Zep, Alcohol Sanitizer Spray, Ethanol 70%, Net Contents 55 Gallons 208 Liters, Made in USA, A Zep Inc. Brand, Distributed by: Zap Inc., 350 Joe Frank Harris Parkway, SE, Emerson, GA 30137, NDC 66949-133-85.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2351-2026·2026-06-17
MIC Safety 20 Fr PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 20 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues. 6,005 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 20 Fr PULL Model/Catalog Number: 8180-20
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2335-2026·2026-06-17
CORFLO Safety PEG kit 30-6312 contains recalled lidocaine injection
CORFLO Safety PEG Kits, catalog number 30-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 31 kits are affected.
Product
Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0912-2026·2026-06-17
Farm Rich Pizza Cheese Crunchers may contain metal pieces
Farm Rich Pizza Cheese Crunchers from Rich Products Corp are being recalled because they may contain metal pieces. The action covers 6,408 cases, or 160,200 lbs.
Product
Farm Rich Pizza Cheese Crunchers
Category
Food
Distribution
21 states
HighFDA (Devices)·Z-2349-2026·2026-06-17
MIC Safety 24 Fr push OTW PEG kits contain recalled lidocaine
MIC Safety PEG Kits with ENFit Connectors, 24 Fr PUSH OTW, catalog number 8170-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PUSH OTW Model/Catalog Number: 8170-24
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2341-2026·2026-06-17
MIC Safety 7170-14 push PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 14 Fr PUSH OTW, catalog number 7170-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 22 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUSH OTW Model/Catalog Number: 7170-14 Product Description: Feeding Tube Kit
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2361-2026·2026-06-17
Medartis APTUS compression screws have off-centre cannulation in affected lots
Medartis APTUS 5.0 headed cannulated compression screws for bone fixation are being recalled because the cannulation of the screw is not centered. 13 units are affected.
Product
Medartis APTUS, 5.0 headedCCS Long Thread 50/20mm, REF A-8216.50/1, 1/Pkg; Cannulated Compression Screws for bone fixation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2339-2026·2026-06-17
CORFLO Safety PEG kit 50-6312 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-6312, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 43 kits affected.
Product
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-6312
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2350-2026·2026-06-17
MIC Safety 14 Fr PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits with ENFit Connectors, 14 Fr PULL, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall for quality issues.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 14 Fr PULL Model/Catalog Number: 8180-14
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2324-2026·2026-06-17
TDC VELOCE 27 gauge vitrectomy cutters may have loose outer knife
TDC VELOCE 27G Two Dimensional Cutters are being recalled following an increase in complaints of a loose outer knife, including reports of it loosening during use.
Product
TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2337-2026·2026-06-17
CORFLO Safety PEG kit 50-4320 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-4320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 49 kits affected.
Product
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-4320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2405-2026·2026-06-17
Abbott Merlin pacemaker programmer may fail to terminate threshold test
Merlin Patient Care System programmer software is being recalled because a malfunction during a pacing capture threshold test may stop the command to terminate the test being communicated.
Product
Merlin" Patient Care System (PCS) software Merlin" PCS 3650 programmer Model 3330 software
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2317-2026·2026-06-17
GE Allia IGS Pulse systems pose shock risk to service personnel
Allia IGS Pulse angiographic X-ray systems are being recalled because an electrical cable issue could expose service personnel to electrical shock while power is on.
Product
Allia IGS Pulse angiographic X-ray system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2338-2026·2026-06-17
CORFLO Safety PEG kit 50-5320 contains recalled lidocaine injection
CORFLO Safety PEG Kits with ENFit Connector, catalog number 50-5320, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 72 kits affected.
Product
Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number: 50-5320
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2352-2026·2026-06-17
MIC Safety 24 Fr pull ENFit PEG kits contain recalled lidocaine
MIC Safety PEG Kits with ENFit Connectors, 24 Fr PULL, catalog number 8180-24, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit Connectors 24 Fr PULL Model/Catalog Number: 8180-24
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2344-2026·2026-06-17
MIC Safety 14 Fr pull PEG kits contain recalled lidocaine injection
MIC Safety PEG Kits, 14 Fr PULL, catalog number 7180-14, are being recalled because they contain lidocaine hydrochloride injection subject to a supplier recall. 208 kits affected.
Product
Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PULL Model/Catalog Number: 7180-14
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2326-2026·2026-06-17
CGuard Prime 8mm carotid stent systems may resist or fail deployment
CGuard Prime Carotid Stent Systems, 135 cm with an 8 mm x 40 mm stent, are being recalled because the delivery system may meet high resistance or fail to deploy the stent.
Product
Brand Name: CGuard¿ Prime Carotid Stent System, 135cm, 8mmx40mm Model/Catalog Number: CND0840
Category
Medical Device
Distribution
Distributed nationwide