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 Sep 21, 2022

Pinnacle3 Radiation Therapy Planning System, Model numbers 870231 and 870237.

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

Philips Medical Systems (Cleveland) Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 21, 2022

QIAcube Connect MDx, Model No. 9003070

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

Qiagen Sciences LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In…

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

Abbott Molecular, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…

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

ICU Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 14, 2022

Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…

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

Philips Respironics, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 14, 2022

Finger Roll 24-pack (033474400885))

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

Piantedosi Baking Co., Inc.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 14, 2022

Early Bird Bleed Monitoring System Introducer Sheath Set, REF: FG001-01 (6F), FG001-02 (8F)

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

Saranas, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 7, 2022

TaperFit Stem, Size 0, 38mm OFFSET, 12/14 Taper + 188.550 Centraliser, For Cemented Use, REF 588.3800. Orthopedic hip…

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

Corin Ltd.

FDA (openFDA device enforcement)

Food

Reported Sep 7, 2022

Wegmans Lemon Dill Finishing Butter, NET WT 3.5 OZ (99g), black plastic cup with a sealed lidding film under the lid.…

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

Epicurean Butter Co.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 7, 2022

Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill…

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

New Standard Device Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 7, 2022

Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.

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

Oculus Optikgeraete GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 7, 2022

Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice,…

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

Woodland Foods LLC

FDA (openFDA food enforcement)

Food

Reported Sep 7, 2022

Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Yem Foods LLC

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 31, 2022

Abbott Jevity Complete, Balanced Nutrition with Fiber Ready to Hang enteral feeding container 1.5 Cal (for tube…

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

Abbott Laboratories

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.

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

bioMerieux, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 31, 2022

Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, packaged in Standup Pouch (24oz). Each case consists of 4/24…

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

Bob's Red Mill Natural Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 31, 2022

(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…

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

GE Healthcare, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.

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

Intera Oncology, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…

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

Medtronic Neuromodulation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

HANA/PROFx CLASSIC FEMORAL HOOK RIGHT REF 6850-144

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

Mizuho OSI

FDA (openFDA device enforcement)

Medical devices

Reported Aug 31, 2022

NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021.

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

Synapse Biomedical Inc.

FDA (openFDA device enforcement)

Drugs

Reported Aug 24, 2022

Avant Foaming Hand Sanitizer, ethanol 62%, a) 18 fl. oz. bottle (530 mL), b) 1000 mL (33.9 fl. oz.) pouch, c) 55 gallon…

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

Aire-Master

5 more products in this recall

FDA (openFDA drug enforcement)

Food

Reported Aug 24, 2022

Ready Meals Shrimp Cooked with Cocktail Sauce SCE NET WT 12 OZ CAL 330 NET WT. 0lb 12oz (340g) ready2eat Tomato paste,…

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

Albertsons Companies LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 24, 2022

(1) CVS Health Sterile Surgical Pads, Cushion Comfort, packaged 12 pads 5 in. x 9 in. per box, ASO Item No. 781083, SKU…

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

Aso LLC

FDA (openFDA device 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.