State

North Carolina product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6651–6675 of 83245

SevereFDA (Devices)·Z-1953-2025·2025-06-18
Tecfen Medical 20G MVR Sideport Knife ophthalmic sterility recall
Tecfen Medical is recalling its 20G (1.2mm) MVR Sideport Knife Straight (Model QKN2312) ophthalmic knives due to sterility assurance concerns. The recall affects 38 units distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 20G (1.2mm) MVR Sideport Knife Straight Model/Catalog Number: QKN2312 Software Version: No software Product Description: This is an ophthalmic knife (manual( that is to be sterile and packaged individually in Tyvek 1059B. MVR sideport
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1921-2025·2025-06-18
SOLTIVE Premium SuperPulsed Laser System surgical instrument thermal incident
Olympus is recalling the SOLTIVE Premium SuperPulsed Laser System due to risk of thermal incidents including smoke, sparks, burning, or flames during clinical use caused by fiber fracturing.
Product
Brand Name: Powered Laser Surgical Instrument Product Name: SOLTIVE Premium SuperPulsed Laser System Model/Catalog Number: TFL-PLS, TFL-PLS-JA (Japan only); Software Version: N/A Product Description: SOLTIVE Laser Systems use technology to increase procedural efficiency and f
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0035-2025·2025-06-18
Jean's Classy Fresh Salsa Recalled Due to Salmonella Contamination
Jean's Classy Fresh Salsa, Mild (5 lbs.) is being recalled due to Salmonella contamination. The product was distributed to Maryland, Pennsylvania, North Carolina, Virginia, and New Jersey.
Product
Jean's Classy Fresh Salsa, Salsa, Mild 5 lbs. 1 per case .
Category
Food
Distribution
5 states
SevereFDA (Food)·H-0021-2025·2025-06-18
Sysco Created Fresh Tuna Salad Subs Recalled for Salmonella Risk
Sysco Corporation is recalling Created Fresh Sub-Tuna Salad on Everything Ficelle (5.76 oz.) due to potential Salmonella contamination from cucumbers used in the product.
Product
HKSAN167 1/5.76 OZ. EA CREATED FRESH Sub- Tuna Salad on Everything Ficelle ALL LOT CODES HKSAN167 1/5.76 OZ. EA Created Fresh Sub- Tuna Salad on Everything Ficelle ALL LOT CODES
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0036-2025·2025-06-18
Cucumber Sliced Unpeeled recalled for Salmonella contamination
TGD Cuts, LLC is recalling Cucumber Sliced Unpeeled (5 lbs. per case, Item #6073) distributed to MD, PA, NC, VA, and NJ due to Salmonella contamination.
Product
Cucumber Sliced Unpeeled, Pack Size 5 lbs. , 1 per case
Category
Food
Distribution
5 states
SevereFDA (Food)·H-0024-2025·2025-06-18
East Coast Fresh Greek Pasta Salad Kit recalled for Salmonella risk
Sysco Corporation is recalling East Coast Fresh Greek Pasta Salad Kits due to potential Salmonella contamination in cucumbers. No illnesses have been reported.
Product
KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Kit 1/5lb W/Pasta ALL LOT CODES KITGREEKPASTA5 1/5# EAST COAST FRESH PC-Greek Pasta Salad Kit 1/5lb W/Pasta ALL LOT CODES KITGREEKPASTA51 1/5# EAST COAST FRESH Greek Pasta Salad Kit 1/5lb W/Pasta (RF) ALL LOT CODES
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0029-2025·2025-06-18
Lipman Family Farms Sliced Cucumbers Recalled for Potential Salmonella
Lipman Family Farms is recalling sliced cucumbers due to potential Salmonella contamination. The product was distributed across multiple states, and consumers should not consume it.
Product
PR Cucumber Sliced 2/5# 1/4 Pack Date May 22 Product of USA Lipman Family Farms Hendersonville / NC
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0026-2025·2025-06-18
Cucumbers Recalled Due to Potential Salmonella Contamination
Lipman Family Farms is recalling 24-count repacked cucumbers distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should discard or return affected cucumbers.
Product
Cucumber 24 Ct Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0020-2025·2025-06-18
Created Fresh Chicken Salad Sandwich Recalled for Salmonella Risk
Sysco Corporation is recalling Created Fresh Chicken Salad on Everything Ficelle sandwiches due to potential Salmonella contamination from cucumbers used in the product.
Product
HKSAC168 6/5.76 OZ. CS CREATED FRESH Sub- Chicken Salad on Everything Ficelle- 6/6oz ALL LOT CODES HKSAN168 1/5.76OZ CREATED FRESH Sub- Chicken Salad on Everything Ficelle ALL LOT CODES HKSAC168 6/5.76 OZ. CS Created Fresh Sub- Chicken Salad on Everything Ficelle- 6/6oz ALL LOT C
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0023-2025·2025-06-18
East Coast Fresh Salsa Products Recalled for Potential Salmonella Contamination
Sysco Corporation is recalling multiple East Coast Fresh salsa products distributed across 18 states and Puerto Rico due to potential Salmonella contamination in cucumbers used in the product.
Product
RTSALSA1LB 1# EAST COAST FRESH Salsa Cup - 1 lb ALL LOT CODES SAL20 5# EAST COAST FRESH EC-Salsa- Fresh 5# ALL LOT CODES SAL210 6/1# EAST COAST FRESH Salsa- Fresh Retail 6x1# (E) ALL LOT CODES SAL45 20# EAST COAST FRESH EC-Salsa- Fresh 20# ALL LOT CODES SAL48 7# EAST COAST FRESH
Category
Food
Distribution
18 states
SevereFDA (Food)·H-0030-2025·2025-06-18
Cucumber Super Selec from Lipman Produce Recalled for Salmonella Risk
Lipman Family Farms is recalling Cucumber Super Selec products due to potential Salmonella contamination. The affected cucumbers were distributed across multiple states.
Product
Cucumber Super Selec Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
Category
Food
Distribution
18 states
SevereFDA (Devices)·Z-1969-2025·2025-06-18
Azurion R1.x and R2.x X-ray systems software communication issue
Philips Medical Systems has recalled Azurion R1.x and R2.x X-ray systems worldwide due to a software issue that can cause loss of imaging functionality and delay treatment, potentially resulting in serious harm or death in patients undergoing urgent or complex interventions.
Product
Azurion R1.x and R2.x systems; Model Numbers: (1) 722063, (2) 722064, (3) 722067, (4) 722068, (5) 722078, (6) 722079, (7) 722221, (8) 722222, (9) 722223, (10) 722224, (11) 722225, (12) 722226, (13) 722227, (14) 722228, (15) 722280, (16) 722281, (17) 722282; Software Version: Al
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1928-2025·2025-06-18
Philips Achieva XR MRI systems recall for fire hazard
Philips Achieva XR MRI systems may have a gradient coil component failure that can generate heat, smoke, and fire. The risk to patients and operators includes inhalation of smoke, burns, and asphyxia.
Product
Achieva XR Product Numbers: (1) 781153, (2) 781253;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1929-2025·2025-06-18
Philips Intera 1.5T Achieva IT Nova MRI System Gradient Coil Fire Risk
Philips is recalling one Intera 1.5T Achieva IT Nova MRI system due to a gradient coil component that may overheat and produce smoke or fire, posing risks of inhalation injury, burns, or death.
Product
Intera 1.5T Achieva IT Nova Product Number: 781175
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1868-2025·2025-06-18
Z-800WF Infusion System software verification defect recall
Zyno Medical LLC is recalling 613 units of the Z-800WF Infusion System because unreleased software versions were installed on distributed devices without verification or validation.
Product
Z-800WF Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0018-2025·2025-06-18
Sysco Corporation Cucumbers Recalled for Potential Salmonella Contamination
Sysco Corporation is recalling cucumber products sold under the Imperial Fresh, East Coast Fresh, Just Cut, Wellsley Farms, and other brands due to potential Salmonella contamination. The products were distributed to multiple states and Puerto Rico.
Product
3909520 2/5# IMPERIAL FRESH CUCUMBER DICED 3/8 SK-ON ALL LOT CODES 480414 2/5 # IMPERIAL FRESH FC CUCUMBER STRIPED AND SLICED ALL LOT CODES 481768 12/3 OZ IMPERIAL FRESH FC VEG VEGGIE W/HUMMUS SMALL P ALL LOT CODES 511666 2/5 # IMPERIAL FRESH FC CUCUMBER SLICED SKIN ON ALL LOT CO
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-1974-2025·2025-06-18
BD TEXIUM Closed Male Luer Devices Recalled for Leaking Interface Risk
BD TEXIUM closed male luer drug transfer devices may leak at the interface between the closed male luer component and the needle-free connector, potentially causing procedure delays, treatment interruptions, hazardous drug exposure, and medication underdosing.
Product
BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP, REF: 10012241; BD TEXIUM (China), REF: 10012241 CHINA
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V416000·2025-06-18
REV Recalls 2025-2026 Fleetwood and Holiday Rambler Motorhomes for Electrical Defect
REV is recalling 2025-2026 Fleetwood Altitude and Holiday Rambler Incline motorhomes because water intrusion may cause electrical components to fail, potentially disabling carbon monoxide or propane detectors.
Product
FLEETWOOD — FLEETWOOD, HOLIDAY RAMBLER ALTITUDE, INCLINE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Food)·H-0025-2025·2025-06-18
Created Fresh Southwest Breakfast Bowl recalled for potential Salmonella contamination
Sysco Corporation is recalling Created Fresh Southwest Breakfast Bowl units because cucumbers in the product have the potential to be contaminated with Salmonella.
Product
HKBKF04 1/11.25 OZ. EA Created Fresh Breakfast Bowl-Southwest ALL LOT CODES
Category
Food
Distribution
18 states
HighNHTSA·25E038000·2025-06-18
Chrysler Recalls Mopar Center Stack Displays Due to Rearview Camera Failure
Chrysler is recalling Mopar Center Stack Displays with a software error that may prevent the rearview camera image from displaying, increasing crash risk.
Product
EQUIPMENT:ELECTRICAL:INFOTAINMENT recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1933-2025·2025-06-18
Philips Intera 1.5T MRI Systems Gradient Coil Fire Risk Recall
Philips is recalling two Intera 1.5T MRI systems due to a gradient coil component failure that can produce smoke or fire, posing risks of inhalation injury, burns, asphyxia, or death.
Product
Intera 1.5T Master/Nova Product Number: 781106;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-0019-2025·2025-06-18
Sysco fresh salad products recalled for potential Salmonella contamination
Sysco Corporation is recalling multiple fresh salad products because cucumbers used in the products have the potential to be contaminated with Salmonella. The recall affects salads sold under brands including East Coast Fresh and Created Fresh.
Product
5185 2/7.125# EAST COAST FRESH AUTHENTIC GREEK SALAD (4070 2/7.125# ALL LOT CODES HKSAL138 1/8 OZ. EA JACK AND OLIVE Salad- House- JO ALL LOT CODES HKSAL176 6/8 OZ. CS CREATED FRESH Salad- House- 6/8oz ALL LOT CODES HKSAL43 2/ 5 LB. CS CREATED FRESH Salad- Kit- Tomato Cucumber 2
Category
Food
Distribution
18 states
HighFDA (Devices)·Z-1938-2025·2025-06-18
MUSE 5 Cardiovascular Systems Recall Administrator Credential Access
GE Medical Systems is recalling MUSE 5 Systems due to a vulnerability that could allow unauthorized access to patient data. The MUSE Administrator Account credentials could potentially be used to log into affected systems from the local network and manipulate recorded cardiovascular patient data.
Product
MUSE 5 Systems, Model Numbers 2021274-001, 2023032-005, 2027478-001, Large capacity client-server-based computer system that accesses stores and manages cardiovascular information.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0935-2025·2025-06-18
Instant Milk Tea Brown Sugar Powder recalled for undeclared milk allergen
R&M Refresher brand Instant Milk Tea Brown Sugar Flavor is recalled because the ingredients contain milk (Whey Powder, Sodium Caseinate) but the label does not declare milk as an allergen.
Product
Instant Milk Tea Brown Sugar Flavor, R&M Refresher brand, B0D725TXQW, net wt. 1lb. Product is sold in 3-pack. Parent ASIN #B0D728CZWS 3-pack ASIN #B0D72FQVDR Ingredients: Non-Dairy Creamer (Glucose Syrup, Vegetable Oil, Whey Powder, Sodium Caseinate***). Product of China. Dis
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1954-2025·2025-06-18
Tecfen Medical 2.0mm Crescent Knife Ophthalmic Device Recall
Tecfen Medical is recalling 2.0mm Crescent Knife ophthalmic surgical instruments (Model QKN1010, Lot ZGY24071501-03) due to sterility assurance concerns. The affected devices were distributed in the US and internationally.
Product
Brand Name: Tecfen Medical Product Name: 2.0mm Crescent Knife Angled Bevel Up Model/Catalog Number: QKN1010 Software Version: No software Product Description: This is an ophthalmic knife (manual) that is to be sterile and packaged individually in Tyhvek 1059B. The crescent kn
Category
Medical Device
Distribution
Distributed nationwide