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 48,100 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Food

Reported Oct 26, 2022

Seeking Health brand Optimal Multivitamin Chewable Dietary Supplement tablets, 60 chewable tablets per package. Product…

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

Seeking Health LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 19, 2022

Veritas Advanced Infusion Packs. Used in ophthalmic procedures.

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

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 12, 2022

Ivenix Infusion System (IIS), LVP Software; LVP-SW-0004 version 5.2.0

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

Fresenius Kabi USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 12, 2022

The BioZorb LP Marker is an implantable radiopaque marker used to facilitate visualization of a soft tissue site. The…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Food

Reported Oct 12, 2022

"Mighty Sesame 10.9oz Organic Tahini" in a 10.9oz plastic squeeze bottle, 8 Units per Cases .

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

Kenover Marketing Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 12, 2022

MR Patient Care Portal 5000 (Desktop Unit), Model Number 453564792561 This is a component of product number 866162.

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

Philips North America LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 12, 2022

Philips Respironics Amara View Minimal Contact Full-Face Mask

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

Philips Respironics, Inc.

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 12, 2022

WFM 365 Organic Creamy Caesar, 12oz, UPC#: 99482490029, Keep Refrigerated. Bottled in USA. Distributed by: Whole Foods…

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

Vanlaw Food Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 5, 2022

VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog No.: EVLT55OPS (each box contains 5 Procedure Kits). For…

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

Angiodynamics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Barco Medical Network Adapter, MNA-240, part of the NexxisOR system, Model Numbers: a) K9303078A, b) K9303097A

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

Barco Nv

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx.

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Humidifier bottle and syringe filter kit (6 count of each) for the BT37 Mark I Benchtop Incubator (AY102295). The Mark…

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

CooperSurgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.

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

DICOM Grid, Inc. d/b/a Ambra Health

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…

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

MEDLINE INDUSTRIES, LP - Northfield

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA10003 OSSUR Power Knee REF PKA01001L OSSUR Power Knee REF…

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH, REF Number 3373-91

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

SunMed Holdings, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 5, 2022

t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…

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

Tandem Diabetes Care Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 5, 2022

Dutch Red Potatoes with Dijon Mustard Sauce. NET WT. 1 LB 1.7 OZ (502g) UPC code 0-45255-15221-0 Distributed by World…

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

World Variety Produce Inc. dba Melissa's

FDA (openFDA food enforcement)

Medical devices

Reported Sep 28, 2022

BD MaxGuard Extension Set with 4-way stopcock, REF: M4058

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

Carefusion

8 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 28, 2022

ANKUR Golden Raisin; 14 Oz (400 gm); UPC Code 8904 1740 10327; packaged in clear plastic bag, 20 bags per wholesale case

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

Muktanand Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 28, 2022

Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture…

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

Paragon 28, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…

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

ICU Medical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 21, 2022

Capri Sun, Wild Cherry, Flavored Juice Drink Blend in 6floz. foil pouch. Sold in carton containing 10 pouches. Carton…

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

Kraft Heinz Foods Company

FDA (openFDA food enforcement)

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Other states

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.