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.
Reported Oct 4, 2017
Bard Magic 3 Antibacterial Hydrophilic Intermittent Catheter Female, 14 FR (30/box), Rx Only intended for urinary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Oct 4, 2017
FRESH FOODS MARKET Artisan Humus Pine Nuts NET WT 10 oz (283g)
High riskUsing this product could cause serious injury, illness or death — stop using it now.House Of Thaller Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 27, 2017
Big Win Butter Popcorn, 5 oz., Butter Popcorn Artificially Flavored; Uncle Ray's 10 oz., Gourmet Select 12 oz., Gold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dedinas Franzak Enterprises dba Cheeze Kurls Inc.c.
FDA (openFDA food enforcement)
Reported Sep 27, 2017
K-Assay(R) Multi-Analyte Calibrator, REF KAI--016C, KAMIYA BIOMEDICAL COMPANY, Seattle, WA, IVD The K-ASSAY(R)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kamiya Biomedical Company, LLC
FDA (openFDA device enforcement)
Reported Sep 27, 2017
Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Java Monster Loco Moca Coffee & Energy, Net Wt. 15 fl. oz. (443 mL); UPC 0 70847 81271 5; INGREDIENTS: BREWED COFFEE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Monster Energy Company
FDA (openFDA food enforcement)
Reported Sep 20, 2017
Wegmans Assorted Muffins 4-Pack-18 oz. (1 lb. 2 oz.) 510g packaged in clear plastic shell. UPC: 77890-22744 .
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wegmans Food Markets, Inc.
FDA (openFDA food enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 13, 2017
JTS External Drive Unit JTS Distal Femoral Extendible Implant Femur is intended for the replacement of diseased or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stanmore Implants Worldwide Ltd.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Papayas Maradol cavi, Grown and Packed by: CARICA DE CAMPECHE, DISTRIBUTED BY: AGROSONS LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.Agrosons LLC
FDA (openFDA food enforcement)
Reported Sep 6, 2017
UniCel DxH Slidemaker Stainer Coulter Cellular Analysis System, Software Version 3.2. The DxH Slidemaker Stainer allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 6, 2017
CORN TREATS CONCENTRATED CARAMEL CORN MIX NET WT 1 LB-6 OZ (22 OZ or 623 g) Manufactured by GOLD MEDAL PRODUCTS CO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gold Medal Products Co.
FDA (openFDA food enforcement)
Reported Sep 6, 2017
Mary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g) box; Ingredients: Whole…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mary's Gone Crackers, Inc.
FDA (openFDA food enforcement)
Reported Sep 6, 2017
Michele s Toasted Muesli, 16 oz bags, 12 units per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Michele's Granola LLC
FDA (openFDA food enforcement)
Reported Sep 6, 2017
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 6, 2017
Toshiba America Medical Systems Ultimax Digital Fluoroscopic X-Ray System Model: DREX-UI80 Ultimax is intended for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Convertors Robotic Drape with Attached Leggings; Product is packaged as Single Sterile Drape/8 per Case
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardinal Health 200, LLC
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Various custom surgical kits manufactured for CMS, CUSTOM MEDICAL SPECIALTIES, INC.: (a) CMS-4153-R2 MPM Biopsy TRAY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Custom Assemblies Inc.
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Demakes Enterprises, Inc. Recalls Chicken Sausage Product Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Demakes Enterprises, Inc.
USDA FSIS
Reported Aug 30, 2017
Fairway brand Cookies Blondie, 10 oz. Item Code 268492 XXXXXX or 263413 XXXXXX.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairway Group Holdings Corp.
FDA (openFDA food enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Medium Coated Jo-Jo Wedges / 00040 (5lb bags)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penobscot McCrum LLC
9 more products in this recall
FDA (openFDA food enforcement)
Free recall alerts
Get alerted about new New Jersey recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.