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.

4,814 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.

Medical devices

Reported Sep 17, 2025

Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID REAMER HEAD Model/Catalog Number: 804-06-311…

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

Encore Medical, LP

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2025

Organic BABY bedtime drops; sleep + immunity blend; Promotes restful sleep with natural herbs & supports immunity with…

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

M.O.M Enterprises, LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 17, 2025

TiBrid Stand Alone Intervertebral Body Fusion Device, SA Angled Punch Awl, Sizes: 30 degree, 45 degree and 60 degree.

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

Omnia Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

QuickVue: Dipstick Strep A Test: 50T, REF: 20108; 25T, REF: 20125; 50T, SCN, REF: 20108SC

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 17, 2025

LinkSymphoKnee System, Tibial Component, Modular, Symmetric, Sz. 5, CoCrMo/TiNbN, cemented, Fixed. REF Number:…

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

Waldemar Link GmbH & Co. KG (Mfg Site)

FDA (openFDA device enforcement)

Food

Reported Sep 17, 2025

Wegmans Medium Camembert Soft Ripened Cheese - 8.8oz - Round wooded container; UPC: 2-77467-00000-7 , 0-77890-53515-8

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

Wegmans Food Markets, Inc.

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2025

Superion IDS Kit Superion Indirect Decompression System 8MM, VF Implant 101-9808 00884662000529 Superion Indirect…

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2025

Evergreen Farm Korean Pear Juice, 4 fl. oz. (120ml) , Foil pouches, 25 foil pouches per case, Refrigerate product after…

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

Evergreen Orchard Farm, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 10, 2025

Hans Kissle Red Bliss Potato Salad

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

Hans Kissle Company, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2025

Brand Name: MediHoney ¿ Product Name: MediHoney¿ Paste Model/Catalog Number: 31505 Product Description: MediHoney¿…

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

Integra LifeSciences Corp. (NeuroSciences)

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 10, 2025

Medshape Universal Joints, REF: DNE-9000-UJ

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

Medshape, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 10, 2025

Nirwana Foods, Golden Raisin, 28 oz (794g), Net Wt. 1.75 LBS, Clear Bags, 20 bags Per Case, keep at room Temperature

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

Nirwana Foods LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 10, 2025

RefleXion X1 Model RXM1000 UDI Codes: (01)00860003983812(11)230504(21)X11001 (01)00860003983812(11)230518(21)X11002…

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

Reflexion Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Baker's Authority Three Seed Mix; 5lb bag; stored dry at room temperature; packaged in silver bag

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

Bakers Authority LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

BD PhaSeal Injector Luer (N30C), REF: 515001 BD PhaSeal Injector Luer Lock (N35), REF: 515003 BD PhaSeal Injector Luer…

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

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

BD Pyxis Product Name / UDI-DI code / Catalog No. BD Pyxis" MedStation" 4000 Main / 10885403512629 / 303 BD Pyxis"…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Deep Sprouted Mat 16 oz.

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

Chetak New York LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

Brand Name: Atlantis IO FLO-S Product Name: Atlantis IO FLO-S Kit Model/Catalog Number: A04B / 68020033 Software…

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

Dentsply IH, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

IPC Powerease System REF 2300000 UDI-DI: 00613994448705 00643169406834. The IPC POWEREASE System is indicated for…

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

Medtronic Xomed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

ELEOS SEGMENTAL LIMB SALVAGE SYSTEM, ELEOS BOWED CANAL FILLING STEMS. Canal filling stem implants.

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

Onkos Surgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 3, 2025

Orascoptic Superior Visualization Custom loupes with Dragonfly frames

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

Orascoptic Surgical Acuity

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 3, 2025

Hostess Ding Dongs CHOCOLATE CAKE WITH CREAMY FILLING 2.55 oz twin pack UPC 8 88109 01002 7; 10-1.28 oz carton (12.7…

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

The J.M. Smucker Company

FDA (openFDA food enforcement)

Medical devices

Reported Sep 3, 2025

Brand Name: THOR Product Name: NovoTHOR Model/Catalog Number: S2188 Software Version: N/A Product Description: The…

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

THOR Photomedicine Ltd.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 27, 2025

Burr Hole Cover Kit, REF: M365DB4600C0; Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep…

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

Boston Scientific Neuromodulation Corporation

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.