State

New Jersey product recalls

72,986 recalls have nationwide distribution and so reach New Jersey. 9,761 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,761
Critical: 1,249
Severe: 2,484
Most recent: 2026-09-25

Of the 9,761 recalls naming New Jersey we have scored against our rubric, 1,249 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,484 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,761 recalls whose distribution notice names New Jersey specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6751–6775 of 82747

SevereFDA (Devices)·Z-1869-2025·2025-06-18
Blood Products Administration Set Filter Mis-Assembly Recall
Fresenius Kabi USA is recalling IVENIX INFUSION SYSTEM LVP Blood Products Administration Sets due to a mis-assembly error that may prevent the drip chamber filter from properly filtering large blood particulates.
Product
IVENIX INFUSION SYSTEM LVP Blood Products Administration Set, Dual-Inlet, Low-Sorbing, Y-Site, Mesh Filter, 15 mL. Intravascular Administration Set.
Category
Medical Device
Distribution
18 states
SevereFDA (Food)·H-0027-2025·2025-06-18
Cucumber Super Selec Repacked by Lipman Produce Recalled for Salmonella
Lipman Family Farms is recalling Cucumber Super Selec products due to potential Salmonella contamination. The 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 (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 (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-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-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-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 (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
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 (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
SevereCPSC·25342·2025-06-18
AstroAI 4-Liter/6-Can Minifridges Recalled Due to Fire and Burn Hazards
AstroAI is recalling approximately 249,100 minifridges because the electrical switch can short circuit, causing fires and burn hazards. At least 70 incidents of smoking, burning, melting, or fire have been reported, including two fires that caused more than $360,000 in property damage.
Product
4 Liter/6 Can Minifridges
Category
Consumer Product
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1931-2025·2025-06-18
Philips Intera 1.5T Achieva Nova-Dual MRI System Fire Hazard Recall
Philips is recalling three Intera 1.5T Achieva Nova-Dual MRI systems worldwide due to a gradient coil component failure that can generate smoke and fire, posing risks including burn injury and asphyxia.
Product
Intera 1.5T Achieva Nova-Dual Product Number: 781173;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·H-0028-2025·2025-06-18
Cucumber 5lb Cases Recalled Due to Potential Salmonella Contamination
Lipman Family Farms is recalling Cucumber 5lb cases distributed across 18 states due to potential Salmonella contamination. Consumers should not consume the product and should dispose of it or return it to the retailer.
Product
Cucumber 5lb Repacked by Lipman Produce Hendersonville, NC 28792, Product of USA
Category
Food
Distribution
18 states
SevereFDA (Devices)·Z-1865-2025·2025-06-18
Z-800 Infusion System recalled for unverified software installation
Zyno Medical LLC is recalling 613 units of the Z-800 Infusion System distributed nationwide because unreleased software versions were installed on the devices without verification or validation.
Product
Z-800 Infusion System. Intended to provide intravenous infusion of parenteral fluids, blood, and blood products to a patient.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0465-2025·2025-06-18
Dietary Supplement Electro Buzz Recalled for Undeclared Active Pharmaceutical Ingredients
SAINI TRADE INC is recalling ELECTRO BUZZ dietary supplement (lot KT-1ST-43-01-07/2024, expiring 10/15/2026) distributed nationwide. Laboratory testing found undeclared chloropretadalafil, propoxyphenylsildenafil, and sildenafil.
Product
ELECTRO BUZZ, Dietary Supplement, 10 capsules per box, Distributed By: Health Fixer, Tempe, AZ 85288, UPC B0DK68LF6J.
Category
Drug
Distribution
Distributed nationwide
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 (Drugs)·D-0463-2025·2025-06-18
Dietary Supplement Male Ultra Recalled for Undeclared Drug Ingredients
Male Ultra dietary supplement, distributed nationwide in 3,000 boxes, has been recalled because laboratory testing found it contains undeclared pharmaceutical ingredients: propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
Product
Male Ultra, Unleash Your Force, Dietary Supplement,10 capsules per box, Distributed By; Health Fixer, Tempe, AZ 85288, UPC B0CMQ4FTHG.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1936-2025·2025-06-18
Philips SmartPath to dStream 1.5T MRI Gradient Coil Fire Risk
Philips SmartPath to dStream for 1.5T MRI systems are recalled due to potential gradient coil component failure that may produce smoke and fire, posing risks of inhalation injury, burns, asphyxia, and death.
Product
SmartPath to dStream for 1.5T¿; Product Number: 782146;
Category
Medical Device
Distribution
Distributed nationwide
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 (Drugs)·D-0466-2025·2025-06-18
Dietary Supplement ULTRA ARMOR Recalled for Undeclared Drug Ingredients
ULTRA ARMOR dietary supplement, distributed by Health Fixer, is recalled nationwide because it contains undeclared pharmaceutical ingredients propoxyphenylsildenafil and sildenafil. The product was marketed without FDA approval.
Product
ULTRA ARMOR, My Armor My Power, Dietary Supplement, 10 capsules per box, Distributed by Health Fixer, Tempe, AZ 85288, UPC B0CYJ7Y5H9.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0467-2025·2025-06-18
Male Ultra Pro dietary supplement recalled for undeclared pharmaceutical ingredients
Male Ultra Pro capsules are being recalled because laboratory testing found undeclared propoxyphenylsildenafil and sildenafil. The product was marketed without an approved New Drug Application.
Product
Male Ultra Pro, Unleash Your Force 2, 10 capsules per box, Distributed by: Health Fixer Tempe AZ 85288, UPC B0CZN7C6YH.
Category
Drug
Distribution
Distributed nationwide
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-1932-2025·2025-06-18
Philips Intera 1.5T Explorer/Nova Dual MRI Gradient Coil Fire Risk
Philips is recalling one Intera 1.5T Explorer/Nova Dual MRI system due to a gradient coil component that may overheat, produce smoke, or ignite, risking patient and operator injury.
Product
Intera 1.5T Explorer/Nova Dual Product Number: 781108;
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1930-2025·2025-06-18
Philips Intera 1.5T Achieva Nova MRI Systems Gradient Coil Fire Risk
Philips is recalling certain Intera 1.5T Achieva Nova MRI systems due to a gradient coil component that can overheat, potentially causing smoke or fire with risk of burns, smoke inhalation, or asphyxia.
Product
Intera 1.5T Achieva Nova Product Number: 781172;
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