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 48,132 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Sep 23, 2015
The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2015
Dexmethylphenidate HCl Extended-Release, Capsules, 10mg, Rx only, 100 Capsules. Manufactured by Alkermes Gainesville…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Novartis Pharmaceuticals Corp.
FDA (openFDA drug enforcement)
Reported Sep 16, 2015
MEDIVATORS HEMOCOR HPH700, HPH-1400TS, HPH-1000TS. Enables the perfusionist to manage the patient's hematocrit and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Perfusion Systems
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2015
ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent; SMN 10316877. Used to prepare the Red Blood Cell hemolysate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2015
CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 16, 2015
2.4, 3.0, and 4.0 mm Gridlock Screw Driver Bit, Model Number 310-30-003, Lot Number TSL002605, NON-STERILE. For use…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Sep 9, 2015
FIRMap 60mm Catheter; Size: 60 mm; Length 50.4 inches French Size Diameter: 8.5F (2.84mm) Model number : USAR064060…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Electrophysiology
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Magic3 Intermittent Catheter with Sure Grip Hydrophilic Coated Silicone Coude tip, Product Code 50614. The catheters…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Soybean sprouts, 1, 2 & 10-lb clear plastic bags labeled GOODSEED Soy Bean Sprouts Keep Refrigerated
High riskUsing this product could cause serious injury, illness or death — stop using it now.Good Seed, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 9, 2015
think Thin Protein & Fiber Oatmeal, Madagascar Vanilla, Almonds, Pecans; 10 g Protein, 5 g Fiber, 190 calories; Net wt…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Interpac Technologies
FDA (openFDA food enforcement)
Reported Sep 9, 2015
Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml (2 vials each of Level 1, Level 2 and Level 3). Also sold…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pointe Scientific, Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Sep 9, 2015
7 Hole VL Gridlock Fibula Plate, Part # 300-60-001 NON-STERILE SINGLE USE ONLY; 9 Hole VL Gridlock Fibula Plate, Part #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Sep 2, 2015
HardyCHROM MRSA Cat no: G307 Lot no: H15155 Expires: 2015-08-13 Container Type: 15x100mm monoplate Packaged: 10…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hardy Diagnostics
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Kale Crisps Zen Nori product is seaweed flavored dehydrated kale chip, sold under brand Veggie Evolution, each poly…
High riskUsing this product could cause serious injury, illness or death — stop using it now.It Takes A Village Foods, LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2015
Cyanocobalamin 500 mcg/mL Injectable, 1 mL pre-filled syringe, Rx only, Liberty Drug Compound Center, 195 Main St., PO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Liberty Drug & Surgical
24 more products in this recall
FDA (openFDA drug enforcement)
Reported Sep 2, 2015
PTW UNIDOS webline: 1) REF T10023, 2) REF T10022 and 3) REF T10023 Firmware version 2.05. Dosimeter for radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PTW-Freiburg
FDA (openFDA device enforcement)
Reported Sep 2, 2015
3.0/4.0 Cannulated Drill Bit; a component of the Tiger Cannulated Screw System The Tiger Cannulated Screw Fixation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
American Science & Engineering Inc,Gemini Cabinet X-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Science & Engineering, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Friendly's Vienna Mocha Chunk Ice Cream Tub, 48 U.S. FL. OZ. UPC: 0-29839 00557-4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Friendly Ice Cream Corp.
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Frozen Jamba, Fruit & Veggie Smoothies, Green Fusion, Green Apple, Mango, Pineapple, Kiwi, Banana, Broccoli and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Inventure Foods
64 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Bronchial Double Lumen Tube Set (Left), Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex, Inc.
8 more products in this recall
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.