State

New Jersey product recalls

72,820 recalls have nationwide distribution and so reach New Jersey. 9,751 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,751
Critical: 1,249
Severe: 2,480
Most recent: 2026-09-09

Of the 9,751 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 2,480 (25%) are Severe.

Which agencies issued them

These figures cover only the 9,751 recalls whose distribution notice names New Jersey specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51–75 of 82571

SevereFDA (Drugs)·D-0790-2026·2026-09-02
Zicam Cold Remedy Nasal Swabs Recalled for Microbiological Testing Failures
Church & Dwight is recalling Zicam Cold Remedy Nasal Swabs because FDA inspections found out-of-limit microbiological testing results at the contract manufacturer.
Product
Zicam, Cold Remedy, Medicated Nasal Swabs, With Cooling Menthol & Eucalyptus, 20 Single-Use Swabs per carton, Zinc-Free Homeopathic, Distributed by Church & Dwight Co. Inc., Ewing, NJ 08628, UPC 732216301205.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1266-2026·2026-09-02
Outshine Fruit Bars Grape Recalled for Potential Glass Contamination
Dreyer's Grand Ice Cream Inc. is recalling Outshine Fruit Bars Grape due to the potential presence of glass pieces.
Product
Outshine Fruit Bars Grape, 6-Count 2.5 ounce, with UPC 041548244044, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Category
Food
Distribution
34 states
SevereFDA (Drugs)·D-0779-2026·2026-09-02
Accord Healthcare Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 100 mcg tablets because they may contain less active ingredient than labeled.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1264-2026·2026-09-02
Outshine Strawberry Fruit Bars Recalled for Potential Glass Contamination
Dreyer's Grand Ice Cream Inc. is recalling Outshine Strawberry Fruit Bars because they may contain glass pieces.
Product
Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual fruit bars in plastic wrapper. Keep at 0F (-18C) or colder.
Category
Food
Distribution
34 states
SevereFDA (Drugs)·D-0778-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium tablets because they may contain less active ingredient than labeled.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0832-2026·2026-09-02
B. Braun Recalls Lactated Ringer's Injection Due to Particulate Matter
B. Braun Medical Inc. is recalling 23,688 bags of Lactated Ringer's Injection USP due to the presence of particulate matter.
Product
LACTATED RINGERS — LACTATED RINGERS (SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3012-2026·2026-09-02
Midmark IQecg Digital ECG Software Recall for Inaccurate Waveforms
Midmark is recalling IQecg Digital ECG software due to a communication anomaly that may cause incorrect waveforms and inaccurate heart rate calculations.
Product
Midmark IQecg Digital ECG, Model/Catalog Number: 4-000-0061, 4-000-0062 Software Version: Midmark IQecg Plugin versions starting with v10 and prior to v10.1.0.18.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3024-2026·2026-09-02
Medline Recalls 663 Surgical Convenience Kits Due to Contamination
Medline Industries is recalling 663 surgical convenience kits distributed nationwide because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: 1) MAJOR GYN PACK, Medline Kit SKU DYNJG001030C; 2) GYN LITHOTOMY PACK, Medline Kit SKU DYNJT8166; 3) OPEN HEART PACK, Medline Kit SKU DYNJ47638B; 4) EAST DAVINCI, Medline Kit SKU DYNJ900949C; 5) THORACIC, Medline Kit SKU DYNJ903470
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3025-2026·2026-09-02
Medline Recalls Gynecologic Robotic Surgery Kits Due to Contamination
Medline Industries is recalling 1,349 gynecologic robotic surgery kits nationwide because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: 1) GYN ROBOTIC CDS, Medline Kit SKU CDS982888Q; 2) GYN ROBOTIC ADD ON PACK, Medline Kit SKU DYNJ43837D; 3) OH GYN/LAP ROBOT PACK, Medline Kit SKU DYNJ89759; 4) GYN LAPAROSCOPY PACK, Medline Kit SKU DYNJ89781; 5) ROBOT ME RF, Medline
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2994-2026·2026-09-02
Medline Medical Convenience Kits Recalled for Endotoxin Levels
Medline Industries is recalling 2,262 medical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Product
Medline medical convenience kits, labeled as: 1) SINUS PACK-LF, Medline Kit SKU DYNJ0966146F; 2) ENT PACK, Medline Kit SKU DYNJ40154D; 3) ENT PACK, Medline Kit SKU DYNJ40154F; 4) ENT SCOPE PACK, Medline Kit SKU DYNJ44480D; 5) ENT NASAL ORAL PACK MOSES, Medline Kit SKU
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3028-2026·2026-09-02
Medline Recalls 419 Surgical Kits Due to Contaminated Component
Medline Industries is recalling 419 surgical convenience kits because they contain a potentially contaminated component. The kits were distributed nationwide.
Product
Medline convenience kits labeled as: 1) CMH LITHO MINOR PACK-LF, Medline Kit SKU DYNJ54362F; 2) EAST MAJOR LITHOTOMY, Medline Kit SKU DYNJ900957C; 3) GYN LAPAROTOMY, Medline Kit SKU DYNJ906804B; 4) UNIVERSAL GYN, Medline Kit SKU DYNJ910195A.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3032-2026·2026-09-02
Healthmark Protein Test Recalled Due to Expired Ingredient
Healthmark is recalling ProChek protein tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Product
healthmark ProChek-W Protein Test for Robotic Arms; ProChek-Semi Quantitative Protein Test, Model Number PT-SQ-001
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26V571000·2026-09-02
Toyota Recalls Multiple Models Due to Inaccurate Load Capacity Labels
Toyota is recalling specific 2024-2026 models because inaccurate load capacity labels may lead to vehicle overloading and increased crash risk.
Product
TOYOTA — 2026 TOYOTA 4RUNNER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3020-2026·2026-09-02
Medline Recalls 263 Surgical Convenience Kits Due to Contamination
Medline Industries is recalling 263 surgical convenience kits because they contain a potentially contaminated component. The kits were distributed nationwide in 18 states.
Product
Medline convenience kits labeled as: 1) OPEN HEART PACK, Medline Kit SKU CDS840393P; 2) OPEN HEART PACK, Medline Kit SKU CDS840393Q; 3) OPEN HEART PROCEDURE, Medline Kit SKU CDS980895W; 4) VALVE CDS, Medline Kit SKU CDS981551G; 5) FEM POP, Medline Kit SKU CDS982028W;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3033-2026·2026-09-02
IMRIS ORT200 Operating Room Table Recalled for Mechanical Failure Risk
IMRIS Imaging Inc is recalling six ORT200 operating room tables because a mechanical failure could cause unintended movement and patient injury.
Product
ORT200, operating room table, including the ORT200 Covered Table Assembly, Reconditioned, Part Number 113821-600 and the ORT200 50/60Hz Covered Table Assy V2 Part Number 114148-000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3026-2026·2026-09-02
Medline C-Section Convenience Kits Recalled for Contaminated Components
Medline Industries is recalling 106 C-section convenience kits distributed nationwide due to potentially contaminated components.
Product
Medline convenience kits labeled as: 1) C-SECTION, Medline Kit SKU DYNJ904612L; 2) C-SECTION, Medline Kit SKU DYNJ911755; 3) AHR C-SECTION KIT, Medline Kit SKU DYNJ912014.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·H-1275-2026·2026-09-02
Lidl Recalls Eridanous Greek Style Shortbread Cookies for Undeclared Allergens
Lidl US Trading is recalling 200 units of Eridanous Greek Style Shortbread Cookies because the labels contain only foreign languages and fail to declare wheat, soy, milk, eggs, and coconut.
Product
ERIDANOUS GREEK STYLE Shortbread Cookies with apricot filling and cocoa topping with coconut sprinkles. Product is packed onto a plastic carton tray with outer paper sleeve, 330 g (weight), UPC: 4056489125846.
Category
Food
Distribution
10 states
HighNHTSA·26V570000·2026-09-02
Toyota Recalls 2026 C-HR Vehicles Due to Battery Overcharge Risk
Toyota is recalling 8,521 2026 C-HR battery electric vehicles because a software error may cause the battery to overcharge, potentially leading to a loss of drive power and increased crash risk.
Product
TOYOTA — TOYOTA C-HR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2992-2026·2026-09-02
Medline Recalls Neonatal Heated Wire Breathing Circuits Due to Thermal Damage
Medline is recalling 145,525 neonatal and infant heated wire breathing circuits due to potential thermal damage that could cause airway obstruction.
Product
Medline breathing circuits labeled as: 1) HUDSON RCI, CIRCUIT, HTD, DL, NEONATE, 48, Medline Product Number/SKU HUD78007 (Teleflex Product Number/SKU 780-07); 2) HUDSON RCI, DBM-CIRCUIT,VENT,NEONATAL,21 V, Medline Product Number/SKU HUD78009 (Teleflex Product Number/SKU 780-
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3031-2026·2026-09-02
Healthmark ProChek-II Medical Tests Recalled for Expired Ingredient
Healthmark Industries is recalling ProChek-II tests because they were manufactured with an expired ingredient, which may cause false negative or positive results.
Product
healthmark ProChek-II, Model Number PT-313, PT-201-12
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0775-2026·2026-09-02
Accord Healthcare Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is voluntarily recalling specific lots of Levothyroxine Sodium 25 mcg tablets nationwide because they are subpotent.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3021-2026·2026-09-02
Medline Head and Neck Kits Recalled for Contaminated Component
Medline is recalling 24 convenience kits labeled as MAJOR HEAD AND NECK PPS because they contain a potentially contaminated component.
Product
Medline convenience kits labeled as: MAJOR HEAD AND NECK PPS, Medline Kit SKU DYNJ9425991S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-3034-2026·2026-09-02
IMRIS ORT300 Operating Room Table Recalled for Mechanical Failure Risk
IMRIS Imaging Inc is recalling 13 ORT300 operating room tables because a mechanical failure could cause unintended rotational movement, posing a risk of injury to patients.
Product
ORT300, operating room table, ORT300 Modular Table Main Unit Assy Part Numbers 114093-000 and 114093-600
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0782-2026·2026-09-02
Accord Recalls Subpotent Levothyroxine Sodium Tablets Nationwide
Accord Healthcare is recalling specific lots of Levothyroxine Sodium 137 mcg tablets because they may contain less than the labeled amount of active ingredient.
Product
LEVOTHYROXINE SODIUM — LEVOTHYROXINE SODIUM (LEVOTHYROXINE SODIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2997-2026·2026-09-02
Medline Neurosurgical Kits Recalled for Endotoxin Contamination
Medline is recalling 974 neurosurgical convenience kits containing neurosponges due to potential out-of-specification endotoxin levels.
Product
Medline medical convenience kits, labeled as: 1) LAMINECTOMY PACK, Medline Kit SKU DYNJT6548; 2) ORTHO SPINE PACK, Medline Kit SKU DYNJ44504G; 3) NEURO SPINE PACK, Medline Kit SKU DYNJ45419F; 4) CRANIOTOMY PACK, Medline Kit SKU DYNJ46024F; 5) SPINE PACK, Medline Kit SK
Category
Medical Device
Distribution
Distributed nationwide