State

New Jersey product recalls

73,376 recalls have nationwide distribution and so reach New Jersey. 9,769 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,769
Critical: 1,249
Severe: 2,939
Most recent: 2026-10-07

Of the 9,769 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 2,939 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,769 recalls whose distribution notice names New Jersey specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19126–19150 of 83145

HighFDA (Devices)·Z-1240-2023·2023-03-22
BD Ultra-Fine Insulin Syringe 0.5mL Recalled for Nonsterility Risk
Becton Dickinson is recalling approximately 1.1 million BD Ultra-Fine Insulin Syringes due to nonsterility concerns. The affected syringes may expose patients to pathogenic microorganisms and risk of local infection.
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 8mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326713
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0582-2023·2023-03-22
Pingo Hot Chocolate Pods Recalled for Undeclared Peanut Residue
Pingo hot chocolate pods may contain undeclared peanut residue. Consumers with peanut allergies should not consume affected products.
Product
Pingo Peanut Butter Cookie Hot Chocolate packaged in single serve pods. Pods are packaged in the following Pingo Variety Pack boxes: Pingo Hot Chocolate Pods Variety Pack, 40 Count UPC: 810683028150 Pingo Hot Chocolate Pods Variety Pack, 100 Count UPC: 810683029805 Pingo Hot…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0439-2023·2023-03-22
Semisweet Chocolate Wafer Recalled for Undeclared Peanut Residue
Clasen Quality Chocolater recalls semisweet chocolate wafers due to undeclared peanut residue that may pose a risk to consumers with peanut allergies. The recall affects 20,000 lbs across 12 states.
Product
Semisweet Chocolate Wafer (FT), Item # 56992. Net Wt. 25 lbs. (11.34 KG) poly-lined case. Ingredients: Sugar, Chocolate Liquor, Cocoa Butter, Sunflower Lecithin (an emulsifier), Vanilla Extract. Distributed By: Clasen Quality Chocolate, 5126 West Terrace Drive, Madison, WI…
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-1254-2023·2023-03-22
Amicus MNC Apheresis Kit at Risk of Stress Leak in Centrifuge Packs
Fenwal Inc is recalling certain batches of the Amicus MNC Apheresis Kit due to a potential for centrifuge packs to develop stress leaks. Affected units were distributed nationwide and internationally.
Product
Amicus MNC Apheresis Kit Double Needle. Component of Amicus Separator multiprocedural apheresis platform
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1244-2023·2023-03-22
BD Ultra-Fine II insulin syringes recalled for sterility defect
Becton Dickinson recalled 1,472,400 BD Ultra-Fine II insulin syringes due to a sterility defect. The nonsterile syringes pose a risk of local infection at injection sites.
Product
BD Ultra-Fine II Insulin Syringe 0.5mL, 8mm, 30G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326725
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0459-2023·2023-03-22
Alprazolam Tablets Recalled Due to Potential Cross-Contamination Risk
Breckenridge Pharmaceutical is recalling multiple lots of Alprazolam 0.5mg tablets nationwide due to manufacturing process deviations that created a potential cross-contamination risk.
Product
Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0431-2023·2023-03-22
Semisweet Chocolate Drops Recalled Due to Undeclared Peanut Residue
Clasen Quality Chocolater, Inc. is recalling 4M Simply Free Semisweet Chocolate Drops because the chocolate may contain undeclared peanut residue, posing a serious risk to consumers with peanut allergies.
Product
4M Simply Free Semisweet Chocolate Drop (FT), Item # 53385. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Chocolate Liquor, Cocoa Butter, Sunflower Lecithin (an emulsifier), and Vanilla Extract. Distributed By: Clasen Quality Chocolate, 5126 West Terrace…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0581-2023·2023-03-22
Coffee pods with undeclared peanut residue being recalled
Two Rivers Coffee is recalling Brooklyn Bean Peanut Butter Cup Hot Cocoa pods because they may contain undeclared peanut residue. Consumers with peanut allergies should not use affected pods.
Product
Brooklyn Bean Peanut Butter Cup Hot Cocoa packaged in single serve pods. Pods are packaged in the following Brooklyn Beans Variety Pack boxes: Brooklyn Beans Hot Chocolate Variety Pack Pods, 12 Count UPC:810683021977 Brooklyn Beans Brooklyn Beans Peanut Butter Chocolate Hot…
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0460-2023·2023-03-22
Alprazolam Tablets Recalled for Potential Cross-Contamination from Manufacturing Deviations
Breckenridge Pharmaceutical is recalling Alprazolam 1 mg tablets distributed nationwide due to manufacturing practice deviations that pose a potential cross-contamination risk.
Product
Alprazolam Tablets, USP, 1 mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0706-01), b) 500-count bottle (NDC 51991-0706-05) and c) 1,000-count bottle (NDC 51991-0706-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0426-2023·2023-03-22
DF FT Simple Free Dark Wafer chocolate recalled for undeclared peanut residue
Clasen Quality Chocolater is recalling DF FT Simple Free Dark Wafer chocolate because it may contain undeclared peanut residue. Consumers with peanut allergies should not consume this product.
Product
DF FT Simple Free Dark Wafer (MB), Item # 12957. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernal Oil, Cocoa Powder, Sunflower Lecithin (an emulsifier), and Salt. Distributed By: Clasen Quality Chocolate, 5126 West Terrace Drive, Madison, WI…
Category
Food
Distribution
12 states
HighFDA (Food)·F-0608-2023·2023-03-22
Sunflower Lecithin Liquid Products Recalled for Undeclared Peanut Allergen
Navada Imports is recalling sunflower lecithin liquid in bulk totes due to undeclared peanut allergen. The affected products were distributed nationwide to food manufacturers.
Product
Sunflower Lecithin Liquid Packaged in 2,200 lb. (1,000 kg.) totes
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0617-2023·2023-03-22
Creamy Ranch Snack Mix Recalled for Metal Contamination
Catalina Snacks recalls Creamy Ranch flavored snack mix due to metal contamination. Consumers who have this product should not eat it.
Product
Creamy Ranch flavored ready-to-eat snack mix packaged in 6oz (UPC 850017468160) plastic stand up pouch.
Category
Food
Distribution
21 states
HighFDA (Drugs)·D-0458-2023·2023-03-22
Alprazolam Tablets Recalled for Potential Cross-Contamination Risk
Breckenridge Pharmaceuticals is recalling Alprazolam Tablets, USP 0.25mg distributed nationwide due to a potential cross-contamination risk from manufacturing deviations.
Product
Alprazolam Tablets, USP, 0.25mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0704-01), b) 500-count bottle and c) 1,000-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc.…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1242-2023·2023-03-22
BD Insulin Syringes Recalled for Nonsterile Condition and Infection Risk
Becton Dickinson is recalling 686,500 units of BD insulin syringes due to a nonsterile condition that may expose patients to pathogenic microorganisms and risk of infection.
Product
BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Single Unit Scale-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329461
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1247-2023·2023-03-22
TFN-Advanced Femoral Nails May Have Incorrect Length Markings
Synthes TFN-Advanced Femoral Nails labeled as 200mm may measure 170mm, and vice versa. Healthcare providers should verify actual dimensions before surgical use.
Product
TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 170MM - STERILE. Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.212S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0469-2023·2023-03-22
Eye allergy medication recalled for out-of-specification impurity
Teva Pharmaceuticals is recalling 715,632 bottles of Clear Eyes Once Daily eye drops due to an out-of-specification impurity found during stability testing.
Product
Clear Eyes, Once Daily, Eye Allergy Itch Relief, olopatadine hydrochloride ophthalmic solution, USP, 0.2%, Antihistamine, 2.5 mL (0.085 fl oz) bottle, Sterile, Distributed by Medtech Products Inc. Tarrytown, NY 10591, A Prestige Consumer Healthcare company, Made in Israel, UPC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1243-2023·2023-03-22
BD Ultra-Fine Insulin Syringes Recalled Due to Nonsterile Condition
Becton Dickinson is recalling BD Ultra-Fine Insulin Syringes (Catalog Number 326719) due to a nonsterile condition that could expose patients to pathogenic microorganisms and local infection. Approximately 80,500 units distributed worldwide are affected.
Product
BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1245-2023·2023-03-22
Fusion Bioline Vascular Graft recalled due to manufacturing straightness defect
Maquet Cardiovascular is recalling one Fusion Bioline Vascular Graft from lot 25162546 that failed straightness testing. The graft could reduce blood flow or cause tension, potentially leading to bleeding and pseudo-aneurysm.
Product
Fusion Bioline Vascular Graft, Part number M00201503046B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0435-2023·2023-03-22
White Confectionery Chocolate Drop May Contain Undeclared Peanut Residue
Clasen Quality Chocolater is recalling 4M White Confectionery Drop MB chocolate because it may contain undeclared peanut residue. Peanut allergen poses a risk to consumers with peanut allergies.
Product
4M White Confectionery Drop MB, Item # 56464. Net Wt. 50 lbs. (22.68 KG) poly-lined case. Ingredients: Sugar, Palm Kernel Oil, Nonfat Dry Milk, Whole Milk Powder, Whey Powder (Milk) Palm Oil, Sunflower Lecithin (an emulsifier), Vanilla Extract. Distributed By: Clasen…
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-1258-2023·2023-03-22
Dimension Tacrolimus Diagnostic Cartridge Recalled for Measurement Imprecision
Siemens is recalling Dimension Tacrolimus diagnostic test cartridges (lots GA2286, GA3047, GA3171) due to confirmed measurement imprecision that could lead to incorrect drug dosing and potential organ failure or toxicity.
Product
Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test for the quantitative measurement of tacrolimus in human whole blood on the Dimension¿ clinical chemistry system SMN: 10700795 (DF207)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0429-2023·2023-03-22
Milk Chocolate Wafers Recalled for Undeclared Peanut Residue
Clasen Quality Chocolate is recalling milk chocolate confectionery wafers due to potential undeclared peanut residue. Consumers with peanut allergies should not consume this product.
Product
Milk Choc Flvd Confectionery Wafer (HP, NSA), Item # 52546. Net Wt. 40 lbs. (18.14 KG) poly-lined case. Ingredients: Palm Kernal Oil, Whey Protein Isolate, Erythritol, Sodium Caseinate, Cocoa Powder (Processed with Alkali), Natural Flavor, Sunflower Lecithin (an emulsifier)…
Category
Food
Distribution
12 states
HighFDA (Devices)·Z-1257-2023·2023-03-22
Beckman Coulter Access Immunoassay Analyzers Recalled for Defective Nut Bands
Beckman Coulter is recalling approximately 4,100 laboratory immunoassay analyzers due to defective nut bands that may cause operational failures and erroneous patient test results.
Product
Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N); (2) Access 2 Immunoassay Analyzer, Refurbished (386220); (3) Access 2 Immunoassay Analyzer, Refurbished (A65531) ; and (4) Access 2 Section, DxC 600i Packaged(A25640).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1237-2023·2023-03-22
BD Ultra-Fine Insulin Syringe Recall Due to Nonsterile Manufacturing
Becton Dickinson is recalling 45,000 units of BD Ultra-Fine Insulin Syringes (catalog 326679, lot 2164338) due to nonsterile manufacturing that could expose patients to pathogenic microorganisms and local infection. Distribution was worldwide.
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326679
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1248-2023·2023-03-22
TFN Femoral Nails dimensions mislabeled, may measure 170mm or 200mm
Synthes recalled TFN-Advanced Femoral Nails because some units have incorrect dimensions: nails labeled 200mm may measure 170mm, while those labeled 170mm may measure 200mm. This dimensional mismatch could compromise surgical fixation.
Product
TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Intended for temporary fixation and stabilization of proximal femur fractures Part Number: 04.037.242S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0438-2023·2023-03-22
Chocolate Baking Chips Recalled Due to Undeclared Peanut Residue
Clasen Quality Chocolater has recalled 4M DF NSA Semisweet Baking Drop chocolate due to potential undeclared peanut residue. The product may pose a risk to consumers with peanut allergies.
Product
4M DF NSA Semisweet Baking Drop (FT), Item # 56854. Net Wt. 40 lbs. (18.14 KG) poly-lined case. Ingredients: Chocolate Liquor, Inulin, Erythritol, Cocoa Butter, Sunflower Lecithin (an emulsifier), Vanilla Extract, Stevia Leaf Reb M. Distributed By: Clasen Quality…
Category
Food
Distribution
12 states