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.

251–275 of 82571

SevereFDA (Drugs)·D-0762-2026·2026-08-19
Shoolin Pharma Recalls Tadalafil USP Due to CGMP Deviations
Shoolin Pharma Chem LLP is recalling Tadalafil USP 1.00 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Product
TADALAFIL USP, 1.00 KG, 1KG(1000gm)-bag, Rx only, "For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO 171596-29-5), NDC 85702-001-08
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0747-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 56,918 vials of Semaglutide 12.5mg due to the presence of nylon and silk particulate matter.
Product
SEMAGLUTIDE 12.5MG (2.5MG/mL), 5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-495-05
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0766-2026·2026-08-19
Prestige Recalls Clear Eyes Maximum Itchy Eye Relief Due to Sterility Concerns
Prestige Brands Holdings is recalling Clear Eyes Maximum Itchy Eye Relief eye drops due to a lack of assurance of sterility and potential contamination.
Product
CLEAR EYES MAXIMUM ITCHY EYE RELIEF — CLEAR EYES MAXIMUM ITCHY EYE RELIEF (GLYCERIN AND NAPHAZOLINE HYDROCHLORIDE AND ZINC SULFATE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1291-2026·2026-08-19
Taylor Farms Recalls Garden Salad Mix Due to Potential Cyclospora Contamination
Taylor Farms is recalling specific lots of garden salad mix and lettuce blends due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.
Product
TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# NATIONAL TAYLOR FARMS BLEND GARDEN SALAD MIX W/ROM 6/5# ND TAYLOR FARMS BLEND LETT/ROM 50/50 NOCLR 4/5# TAYLOR FARMS BLEND LETT/ROM 70/30 NOCOLR 4/5# TAYLOR FARMS BLEND LETT/ROM 80/20 4/5# TAYLOR FARMS LETTUCE SALAD MIX 4/5# Iceberg
Category
Food
Distribution
27 states
SevereFDA (Food)·H-1289-2026·2026-08-19
Taylor Farms Recalls Iceberg and Romaine Lettuce for Potential Cyclospora
Taylor Farms de Mexico is recalling specific lots of iceberg and romaine lettuce blends due to potential Cyclospora contamination.
Product
MARKON BLEND LETT/ROM 50/50 NOCLR 4/5# MARKON BLEND LETT/ROM 80/20 4/5# Iceberg, Romaine products.
Category
Food
Distribution
27 states
SevereFDA (Food)·H-1280-2026·2026-08-19
Taylor Farms Recalls Marketside Iceberg Salad for Potential Cyclospora Contamination
Taylor Farms is recalling specific Marketside iceberg salad products due to potential Cyclospora contamination. Consumers should check lot codes and discard affected items.
Product
MARKETSIDE ICEBERG SALAD 10/24 oz, UPC 681131328951; MARKETSIDE ICEBERG SALAD 12/12 oz, UPC 681131328944; MARKETSIDE SHREDDED LETT 12/16 oz, UPC 681131532099; MARKETSIDE SHREDDED LETT 12/8 oz, UPC 681131328968; Iceberg only products.
Category
Food
Distribution
27 states
SevereFDA (Drugs)·D-0756-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 500 vials of Semaglutide 10mg due to the presence of nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 10mg (5mg/mL), Glycine 10 mg (5mg/mL), 2 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-722-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0752-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.
Product
SEMAGLUTIDE 0.9mg (0.9 mg/mL), 1 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-810-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0753-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling 250 vials of Semaglutide 2.5mg due to the presence of nylon and silk particulate matter.
Product
SEMAGLUTIDE 2.5mg (1mg/mL), Glycine 12.5 mg (5mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-711-02
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0755-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 7.5mg (5mg/mL), Glycine 7.5 mg (5mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202. NDC 71170-721-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0749-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 6.75mg (4.5 mg/mL), 1.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-821-01
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0787-2026·2026-08-19
Baxter Recalls Cefazolin Injection Bags Due to Particulate Matter
Baxter Healthcare is recalling 19,032 bags of Cefazolin Injection due to the presence of particulate matter. The affected product is distributed nationwide in the US.
Product
CEFAZOLIN — CEFAZOLIN (CEFAZOLIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·H-1282-2026·2026-08-19
Taylor Farms Recalls Shredded Iceberg Lettuce Due to Cyclospora Contamination
Taylor Farms de Mexico is recalling specific lots of shredded iceberg lettuce due to potential Cyclospora contamination. The product was distributed across 28 U.S. states and Mexico.
Product
PEAK LETTUCE SHRED 1/8" 4/5# Iceberg only products.
Category
Food
Distribution
27 states
SevereFDA (Drugs)·D-0748-2026·2026-08-19
Apollo Care Recalls Semaglutide Vials Due to Particulate Matter
Apollo Care, LLC is recalling specific lots of Semaglutide 2.25mg vials because they contain nylon and silk-type particulate matter.
Product
SEMAGLUTIDE 2.25MG (0.9 mg/mL), 2.5 mL Sterile Multi-Dose Vial, Rx Only, For Subcutaneous Injection Only, APOLLO care, 3801 Mojave Ct, Ste 102, Columbia, MO 65202 NDC 71170-811-02
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·26V537000·2026-08-19
E-One Recalls Fire Trucks Due to Hydraulic Valve Defect
E-One is recalling specific 2025-2026 fire trucks because a hydraulic valve defect may prevent outriggers from extending or retracting, potentially delaying emergency response.
Product
E-ONE — E-ONE CYCLONE N, CYCLONE II, TYPHOON N
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2946-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability in Sponges
Cardinal Health is recalling 602 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.
Product
Cardinal Health Presource Kits: 1) SEPTO RHINO PACK , Catalog Number: SEN73NSKCF; 2) PACK NEURO MINOR CRANIOTOMY , Catalog Number: SNE30CNOHE; 3) NEURO MAJOR 2 PACK , Catalog Number: SNE30CRJGY; 4) NEURO PACK , Catalog Number: SNE43
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2919-2026·2026-08-19
V-Loc 180 Absorbable Wound Closure Device Recalled for Packaging Defects
FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.
Product
V-Loc 180 Absorbable Wound Closure Device BOX BEDSIDE STAPLING IS KING BOX06614V4 BOX BY PASS FINAL BOX07405V1 BOX BYPASS CARDON BOX01056V2 BOX BYPASS DR LAGAE BOX01482V2 BOX BYPASS KIT DEZEMBER 2025 BOX09222V1 BOX BYPASS KIT NEU BOX 003
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2912-2026·2026-08-19
Microvention Recalls Bobby Balloon Guide Catheters Due to Pinhole Defects
Microvention Inc. is recalling 5,500 Bobby Balloon Guide Catheters worldwide due to an increased rate of balloon pinhole defects.
Product
BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in facilitating the insertion and guidance of an intravascular catheter into a selected blood vessel in the peripheral and neurovascular systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2944-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Product
Cardinal Health Presource Kits: 1) NEWNAN SMR PACK, Catalog Number: SEN21SPPMB
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2925-2026·2026-08-19
Medline Bleach Wipes Recalled for Reduced Disinfection Effectiveness
Medline is recalling bleach wipes that may lose potency before expiration, potentially allowing pathogens to survive.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count, Product Number MSC351450AN
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2926-2026·2026-08-19
Medline Micro-Kill Bleach Germicidal Wipes Recalled for Reduced Concentration
Medline Industries is recalling Micro-Kill Bleach Germicidal Wipes because bleach concentration may drop below specification, potentially compromising disinfection effectiveness.
Product
Medline Micro-Kill Bleach Germicidal Bleach Wipes, 12" x 12", 110 Count Bag, Product Number MSC351450BG4
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2921-2026·2026-08-19
Surgipro Sutures Recalled for Potential Sterile Barrier Perforation
FDA is recalling Surgipro sutures due to potential sterile barrier defects that could cause biocontamination and infection.
Product
Surgipro SP-623 SURGIPRO* 2-0 BLU 75CM SC2 X36 SP-623
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2949-2026·2026-08-19
Cardinal Health Presource Kits Recalled for Endotoxin Variability
Cardinal Health is recalling 616 Presource Kits because they contain sponges with unexpected endotoxin variability.
Product
Cardinal Health Presource Kits: 1) BASIC PACK , Catalog Number: SBA73BPGCA; 2) SPINE PACK , Catalog Number: SNE11SPHKC; 3) SPINE PACK , Catalog Number: SNE11SPHKD; 4) CRANIOTOMY PACK , Catalog Number: S
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·26E059000·2026-08-19
Avride Recalls Automated Driving Systems Due to Unsafe Lane Changes
Avride Inc. is recalling Automated Driving Systems (ADS) with specific software versions that may cause unsafe lane changes or merging without yielding.
Product
ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2766-2026·2026-08-19
Baxter Duo-Vent Solution Set Recalled for Air Bubbles in Tubing
Baxter Healthcare is recalling 24,528 units of Duo-Vent Solution Sets due to customer reports of air bubbles in the drip chamber and tubing.
Product
Baxter Duo-Vent Solution Set and Male Luer Lock Adapter, Product Code 1C8507; Solution Administration Sets
Category
Medical Device
Distribution
Distributed nationwide