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.
Reported Dec 17, 2025
Outer-packaging: gimme! brand Decaf de Agua coffee pods, Net Wt. 4.23 oz, UPC 051497457990, box of 10 pods…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gimme Coffee, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2025
Doughy brand Chocolate Chip Cookie Dough; 12 oz
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hudson River Foods Corp.
FDA (openFDA food enforcement)
Reported Dec 17, 2025
UPC 8 10248 03165 6 YELLOW Peaches PRODUCE OF U.S.A. NET WT. 4 LBS. MOONLIGHT PACKING CORP. REEDLEY, CALIFORNIA 93654…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Moonlight Packing Corporation
10 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 17, 2025
Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nipro Medical Corporation
FDA (openFDA device enforcement)
Reported Dec 17, 2025
Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Orthofix U.S. LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Hemochron Activated Clotting Time Low-Range Test Cuvette, REF: ACT-LR, to be used with the Hemochron Signature ELITE…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accriva Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Organic Moringa Leaf Powder (Moringa Powder) , 4 oz. and 1 Kilogram, 4 oz size in a solid plastic container / 1 kg size…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Africa Imports
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Blonde Beard's Dojo Asian Wing Sauce, wing sauce hot sauce condiment, shelf stable, 2 years, glass bottle, 8 oz, Blonde…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blonde Beard's
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Costco Item# 19927 Kirkland Signature Caesar Salad, refrigerated, packaged in clear plastic clamshell container. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Costco Wholesale Corporation
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 10, 2025
InSure ONE Fecal Immunochemical Test. Labeled as follows: 1. Insure ONE POL Patient Kit - 10 pack. Model Number: 90010.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Enterix, Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Genepro Whey 4th Generation Plasma Treated Protein, unflavored, Net Wt. 225g, 30 servings, packaged in a resealable…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Genepro Protein, Inc.
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Reagent Kits/ containing flow cells, components of NextSeq 550Dx Instrument: NextSeq 550Dx High Output Reagent Kit v2.5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Illumina, Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Loaded Veggie Grain Bowl; NET WT. 10/90 OZ (309g) NO UPC Identifying N4L code: V3FR
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutrition for Longevity
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Phantom Fibula Nail, 2.8mm x 130mm, Right, Ti, Fibula Nail, REF: P36-128-130R-S
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Lumify Diagnostic Ultrasound System models : 795005, 795161, 989605449841,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound, LLC
FDA (openFDA device enforcement)
Reported Dec 10, 2025
Lava Bun with Green Tea Flavor bright lime green packaging (Frozen) Unsalted butter and cream are listed in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Prime Food Processing LLC.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Aojia Dried Red Bayberry; packaged in 5.6oz (160g) clear plastic bottle; UPC 6942514920327
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rong Shing Trading NY Inc.
FDA (openFDA food enforcement)
Reported Dec 10, 2025
Italian Salad Dressing; Net 1 GAL (3.78L) SKU: 7 67367 00518 4 Creamy Poblano Avocado Ranch Dressing and Dip; Net…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventura Foods LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 9, 2025
Ghanaianway Restaurant and Grocery LLC Recalls Fresh Salted Lamb Products Produced Without Benefit of Inspection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ghanaianway Restaurant and Grocery LLC
USDA FSIS
Reported Dec 3, 2025
CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Option"ELITE Vena Cava Filter System REF 352506070E UDI-DI code: 00886333217151 The Option"ELITE Filter is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Dec 3, 2025
BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Dec 3, 2025
Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Djo, LLC
FDA (openFDA device enforcement)
Reported Dec 3, 2025
FoundationOne CDx (F1CDx), RAL-0003 version 31.0
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Foundation Medicine, Inc.
1 more product 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.