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.
4,816 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Jan 15, 2025
EnVisio Patient Pad Transition Cushion, Model/Catalog Number: ENVISIO-SYS Product Description: The EnVisio Patient Pad…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elucent Medical Inc.
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Grecian Delight Tzatziki sauce, 3.75 lb. tub, UPC 07365000286, SKU SAL028, 4 tubs per case. Sysco Classic Tzatziki…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grecian Delight/Kronos
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 15, 2025
Citric Complete - Dry Citric Acid Concentrate Model Number: DCA+225-25
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nipro Renal Soultions USA, Corporation
FDA (openFDA device enforcement)
Reported Jan 15, 2025
Olympia Foods Grecian Dip Tzatziki sauce, item 100, 4 lb. tubs, UPC 10045059001001, 4 tubs per case; item 104, 32lbs…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Olympia Foods
FDA (openFDA food enforcement)
Reported Jan 15, 2025
Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 8, 2025
3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Unitek Corporation
FDA (openFDA device enforcement)
Reported Jan 8, 2025
AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Angiodynamics, Inc.
FDA (openFDA device enforcement)
Reported Jan 8, 2025
--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Grimmway Enterprises, Inc. dba Grimmway Farms
4 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 8, 2025
Sprout Gyro Family Kit, net wt. 1.750 lb (794 g), food, perishable, plastic tray, 28oz, U UPC 20594800000.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sprouts Farmers Market
FDA (openFDA food enforcement)
Reported Jan 1, 2025
The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Medical
FDA (openFDA device enforcement)
Reported Jan 1, 2025
FACSLyric 2L4C Instrument US, Catalog Number 662875, UDI 00382906628756 BD FACSLyric" flow cytometer is intended for in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton, Dickinson and Company, BD Bio Sciences
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 1, 2025
Galaxy System (GAL-001). Intended to provide bronchoscopic visualization of and access to patient airways for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noah Medical
FDA (openFDA device enforcement)
Reported Jan 1, 2025
BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straight Smile, LLC
FDA (openFDA device enforcement)
Reported Jan 1, 2025
ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zoe US, Inc.
FDA (openFDA food enforcement)
Reported Dec 25, 2024
Brand Name: K-Systems Product Name: G73 Dry Bath Incubator Model/Catalog Number: K22065 Product Description: An…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
OEC 3D REF Image-Intensified Fluoroscopic X-Ray System, Mobile. The OEC 3D is a mobile fluoroscopic C-Arm imaging…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE OEC Medical Systems, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Galaxy System (GAL-001)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noah Medical
FDA (openFDA device enforcement)
Reported Dec 25, 2024
Turbo Elite Laser Atherectomy Catheter Model Number / UDI-DI code / Product Description 414-151 / 989930000531 / 1.4 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spectranetics Corporation
FDA (openFDA device enforcement)
Reported Dec 18, 2024
BD Pyxis MedStation ES, REF: 323
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2024
Timolol Maleate Ophthalmic Solution USP, 0.25%, Sterile, 15mL bottles, Rx only, Manufactured by: FDC Limited, Waluj,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.FDC Limited
FDA (openFDA drug enforcement)
Reported Dec 18, 2024
Hybrid Recon software on Hermes Medical Imaging Suite version 6.1 Hybrid Recon software versions affected are 4.0.0x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hermes Medical Solutions AB
FDA (openFDA device enforcement)
Reported Dec 18, 2024
Mama Mancini s Stuffed Shells with Sauce and Mozzarella Cheese, 4 packs of 4 lbs. each / 6 packs of 14 oz. each, 4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Joseph Epstein Food Enterprises, Inc. dba MamaMancini's
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 18, 2024
MICRO-X Rover Mobile X-ray System, # MXU-RV35
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro-X Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 18, 2024
Galaxy bronchoscope (Product GALB-001) used with Instructions for use, Part: 10000752, part of the Noah Medical Galaxy…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Noah Medical
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.