All recall categories

Recalls distributed in New Jersey

These notices name New Jersey in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

4,754 stored notices name New Jersey, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Medical devices

Reported Mar 17, 2021

Dimension Vista HDLC - colorimetric method, lipoproteins - Product Usage: used as an aid in the diagnosis of lipid…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 17, 2021

Thread-like wire marker

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Somatex Medical Technologies GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

ACIST Kodama Intravascular Ultrasound Catheter The Kodama Intravascular Ultrasound Catheter is a component of the ACIST…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Acist Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

Band, Elastic, Orthodontic - Product Usage: Orthodontic elastics, also referred to as rubber bands, are small stretchy…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

G & H Wire Company

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

HAMILTON HEATER SHAKER, 115 VAC/ 230 VAC, 750 VA, Power Consumption 41V/ 100W (max.), Relative Humidity 15% - 85% no…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Hamilton Co.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

WMTS Telemetry Receiver, Multiple Patient Receiver, Model Number/ UDI: ORG 9100A/ 00841983102554 ORG 9110A/…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nihon Kohden America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 10, 2021

Various reprocessed products: PROVISION, Reprocessed Smith and Nephew Arthroscopic Shavers, STERILE EO; PROVISION…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ReNovo, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

Infusion Pump

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

Slush + Warmer Disc Drape; Model ORS-320 Slush + Warmer Disc Drapes - Product Usage: single-use equipment cover…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ecolab Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 3, 2021

Golden Boy Custard Muffin Banana 220 grams/7.76 ounce packages

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Hong Thai Foods Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 3, 2021

VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

ENROUTE Transcarotid Stent System REF SR-XXYY-CS

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Silk Road Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

OT1000 Series Orthopedic Surgical Tables

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Steris Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

IOLMaster 700

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Carl Zeiss Meditec AG

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Confirm Biosciences Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

SenTec Digital Monitor, Model SDM, is a portable stand-alone patient monitor indicated for continuous, noninvasive…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

SenTec AG

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biopsy Needle, 1/7F…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Argon Medical Devices, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cytocell Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Draegar Medical Systems, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 17, 2021

"LAVVA Blueberry Dairy Free Pili Nut Yogurt. NO SUGAR ADDED. NET WT 5.3OZ (150g) ***KEEP REFRIGERATED***DISTRIBUTED BY…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Evr Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 17, 2021

GE Healthcare Precision 600FP, Classical R&F (radiographic and fluoroscopic) System - Product Usage: Intended for use…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

GE Healthcare, LLC

FDA (openFDA device enforcement)

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RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.