State

New Jersey product recalls

73,824 recalls have nationwide distribution and so reach New Jersey. 9,782 additional recalls listed New Jersey specifically in their distribution scope.

What the numbers show

Total: 9,782
Critical: 1,246
Severe: 2,944
Most recent: 2026-11-04

Of the 9,782 recalls naming New Jersey we have scored against our rubric, 1,246 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,944 (30%) are Severe.

Which agencies issued them

These figures cover only the 9,782 recalls whose distribution notice names New Jersey specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44101–44125 of 83606

ModerateFDA (Devices)·Z-1772-2018·2018-05-16
Bard POWERPORT ClearVUE Implantable Port Recall for Incorrect Instructions
Bard Peripheral Vascular Inc is recalling 15 units of POWERPORT ClearVUE isp Implantable Port kits because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1689-2018·2018-05-16
Siemens ADVIA Centaur Folate Recalled for Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Folate assays because biotin interference levels are not listed in the instructions, potentially affecting test accuracy.
Product
ADVIA Centaur¿ Folate (FOL)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1778-2018·2018-05-16
Siemens Syngo.Via Software Recall for Report Functionality Defect
Siemens Medical Solutions is recalling Syngo.Via VB20A software because corrected report values are not saved or transmitted, causing the system to use original values.
Product
Syngo.Via VB20A model 1049610
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1768-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Flushing Instructions
Bard Peripheral Vascular Inc is recalling 3,196 units of POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter, REF 5676300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1764-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Patient Card Instructions
Bard Peripheral Vascular Inc is recalling POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1678300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1403-2018·2018-05-16
Energique Enervimin CNCR Focus Recalled as Unapproved New Drug
Grato Holdings, Inc. is recalling Energique Enervimin CNCR Focus dietary supplements because they are unapproved new drugs based on disease claims.
Product
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1676-2018·2018-05-16
Siemens IMMULITE 2000 Folic Acid Assay Recalled for Biotin Interference
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Folic Acid assays because biotin interference is not listed in the instructions for use.
Product
IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Folic Acid
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1678-2018·2018-05-16
Siemens IMMULITE CEA Assay Recalled for Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling IMMULITE CEA assays because biotin interference thresholds are not listed in the instructions, potentially affecting test accuracy.
Product
IMMULITE ¿ /IMMULITE ¿ 1000 CEA
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1693-2018·2018-05-16
Straumann Emdogain Recalled Due to Unverified Raw Material Shelf Life Changes
Straumann Manufacturing is recalling Emdogain Enamel Matrix Derivative because a raw material shelf life change was implemented without submitting data to demonstrate continued product efficacy.
Product
Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number 075.098W
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1779-2018·2018-05-16
MHC Medical Recalls EasyTouch Insulin Syringes Due to Lot Labeling Error
MHC Medical Products LLC is recalling EasyTouch Insulin Syringes because retail cartons may display incorrect lot numbers.
Product
EasyTouch (ET) Insulin Syringe 29G 1ml ¿" (Item 829155) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1643-2018·2018-05-16
Beckman Coulter iChemVELOCITY Urine Chemistry System Recall for Incorrect Settings
Beckman Coulter is recalling 2,225 iChemVELOCITY Urine Chemistry Systems because incorrect settings may cause false low results or incorrect color reporting.
Product
BECKMAN COULTER iChemVELOCITY, Urine Chemistry System, Catalog Numbers: 800-3530, 800-7167, 800-7719, 800-7720, 800- 7106, 800-3049, 800-3050, 800-3079, 800-3080, 800-7190, 800-7713, 800-7714, 800-7715, 700- 7176-001, 700-7177-001 Product Usage: The iChemVELOCITY…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1767-2018·2018-05-16
Bard Peripheral Vascular Recalls POWERPORT ClearVUE Catheters
Bard Peripheral Vascular Inc is recalling 4,044 POWERPORT ClearVUE catheters because the Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 5668362
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1674-2018·2018-05-16
Siemens IMMULITE 2000 Allergy IgE Kit Recalled for Biotin Interference
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Allergy specific IgE Universal Kits because biotin interference is not documented in the instructions for use.
Product
IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi 3g Allergy specific IgE Universal Kit
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1763-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Patient Card Instructions
Bard Peripheral Vascular Inc is recalling 216 units of POWERPORT ClearVUE Slim catheters because the packaged Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1676301
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0863-2018·2018-05-16
Noven Pharmaceuticals Recalls Minivelle Estradiol Transdermal Patches for Adhesive Defects
Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal patches because the adhesive may not stick well to the skin.
Product
MINIVELLE — MINIVELLE (ESTRADIOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1686-2018·2018-05-16
Siemens IMMULITE Vitamin B12 Assay Recalled Due to Biotin Interference
Siemens Healthcare Diagnostics is recalling IMMULITE Vitamin B12 assays because biotin interference is not listed in the instructions for use.
Product
IMMULITE ¿ /IMMULITE ¿ 1000 Vitamin B12
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1782-2018·2018-05-16
Ondamed Biofeedback Device Recalled for Lack of Marketing Clearance
Ondamed Inc is recalling 585 Ondamed Biofeedback Devices because they were marketed in the US without FDA clearance. Customers are advised to contact the firm for an available upgrade.
Product
Ondamed Biofeedback Device, Model No. 001-00-0101 The product is a battery powered biofeedback device that is indicated for relaxation training and muscle re-education and prescription use.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1682-2018·2018-05-16
Siemens IMMULITE CA125 Assay Recalled for Biotin Interference
Siemens Healthcare Diagnostics is recalling IMMULITE CA125 assays because biotin interference thresholds are not listed in the instructions, potentially affecting test accuracy.
Product
IMMULITE ¿ /IMMULITE ¿ 1000 OM-MA (CA125)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1766-2018·2018-05-16
Bard POWERPORT ClearVUE Implantable Port Recalled for Incorrect Flushing Instructions
Bard Peripheral Vascular Inc is recalling 876 units of POWERPORT ClearVUE Implantable Ports because the packaged Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter, REF 5666362
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1396-2018·2018-05-16
Munk Pack Protein Cookies Recalled Due to Mold Growth
Munk Pack Inc. is recalling specific lots of Protein Cookies due to mold growth. Consumers should check their pantry and discard affected products.
Product
Munk Pack PROTEIN COOKIE PEANUT BUTTER CHOCLATE CHIP NET WT 2.96oz (84g); UPC: 853787005351
Category
Food
Distribution
23 states
ModerateFDA (Devices)·Z-1673-2018·2018-05-16
Siemens Recalls Dimension Vista TSH Reagent Cartridges for Labeling Error
Siemens is recalling Dimension Vista TSH reagent cartridges because the instructions incorrectly state the biotin interference level.
Product
Dimension Vista¿ Thyroid Stimulating Hormone (TSH) Flex¿ reagent cartridge
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1395-2018·2018-05-16
Munk Pack Protein Cookie Recall Issued Due to Mold Growth
Munk Pack Inc. is recalling specific lots of Double Dark Chocolate Protein Cookies due to mold growth. Consumers should check their pantry and discard affected products.
Product
Munk Pack PROTEIN COOKIE DOUBLE DARK CHOCOLATE NET WT 2.96oz (84g); UPC: 853787005368
Category
Food
Distribution
23 states
ModerateFDA (Devices)·Z-1761-2018·2018-05-16
Bard POWERPORT ClearVUE isp Catheter Recalled for Incorrect Instructions
Bard Peripheral Vascular Inc is recalling 2,395 units of POWERPORT ClearVUE isp catheters because the packaged Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE isp with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1668362
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1771-2018·2018-05-16
Bard Peripheral Vascular Recalls POWERPORT ClearVUE Implantable Ports
Bard Peripheral Vascular Inc is recalling 181 POWERPORT ClearVUE Slim catheters because the included Patient ID Card has incorrect flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with open suture holes, REF 5678301
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1769-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Patient Card Instructions
Bard Peripheral Vascular Inc is recalling 835 units of POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter with Open Suture Holes, REF 5676301
Category
Medical Device
Distribution
Distributed nationwide