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.
4,822 stored notices name New Jersey, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New Jersey too — those are in the archive.
Reported Nov 24, 2021
Vit Kit-Freeze is intended for use in assisted reproductive procedures for vitrification and storage of human oocytes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fujifilm Irvine Scientific, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 24, 2021
VITROS Immunodiagnostic Products Anti-HBc IgM Controls, Product Code 6801427 For use in monitoring the performance of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Ortho-Clinical Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Nov 24, 2021
Smith and Nephew EVOS Self-Tapping Locking Screw SST: (1)REF 72413575, 3.5MM x 75MM, and (2) REF 72413570, 3.5MM X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew, Inc.
FDA (openFDA device enforcement)
Reported Nov 24, 2021
Permobil TiLite, Models: Aero Z, and ZRA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TiSport, LLC
FDA (openFDA device enforcement)
Reported Nov 17, 2021
Hemodialysis Delivery System, Software Version 2.x.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
FDA (openFDA device enforcement)
Reported Nov 17, 2021
Sundelight Golden Raisins Net Wt 7oz. UPC: 14760 84059. Plastic pouches. 20 pouches/per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Best Foods NJ, Inc.
FDA (openFDA food enforcement)
Reported Nov 17, 2021
T4 EIA Kit, Cat No: BC-1007, Store at 2-8C, For in vitro diagnostic use only This product s intended use is For the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioCheck, Inc.
FDA (openFDA device enforcement)
Reported Nov 17, 2021
Ingredion INSTANT PURE-FLO F (50 pound bag) food grade starch material 12151103CA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ingredion Incorporated
FDA (openFDA food enforcement)
Reported Nov 17, 2021
NOW Royal Jelly 1500mg 60 VCAPS UPC 733739025654 NOW Royal Jelly 1500mg 60 VCAPS (Distributed by Sofico) UPC…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Health Group Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 10, 2021
3M Red Dot Electrodes, Radiolucent Monitoring Electrode with Foam Tape, Catalog No. 2244, (3M ID (SKU): 70-2011-8506-6,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Nov 10, 2021
Flexor Check-Flo Introducer, Introducer Set, RPN KCFW-6.0-35-45-RB, GPN G09908 The introducer sheath incorporates a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 10, 2021
ImplantDirect, REF 834711, Legacy 2 Implant 4.7mmD x 11.5mmL, 4.5mmD Platform,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 10, 2021
FIVE S 3.5x65, Flexible Intubation Videoscope, REF: 091361-01 (1 Unit), and 091361-06 (6 Units)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
FDA (openFDA device enforcement)
Reported Nov 10, 2021
IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lumenis, Inc.
FDA (openFDA device enforcement)
Reported Nov 10, 2021
Whole raw RED onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ProSource Produce LLC
2 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 3, 2021
Cliquid MD version 3.4 software used in conjunction with Analyst MD software on SCIEX Citrine & 4500MD series liquid…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ab Sciex
FDA (openFDA device enforcement)
Reported Nov 3, 2021
Nature's Heart Superfood Trail Mix 1.5oz poly film pouches - 32 units per case
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nestle USA Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 3, 2021
Simply Nature Organic Poppy Seed Dressing
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Schlotterbeck & Foss LLC
FDA (openFDA food enforcement)
Reported Nov 3, 2021
Almond Flour Crackers fine ground sea salt packaged in a white box with yellow graphics weighing 4.25 oz. Label reads…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Simple Mills
FDA (openFDA food enforcement)
Reported Nov 3, 2021
REF/Catalogue Number GSX0030A, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 27, 2021
Herniatome, 17G x 15cm, Lumbar Type with with 20ga-30cm Introducer, Model Number 5091715
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Adria Srl
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 27, 2021
SIMPLEXA COVID-19 Positive Control Pack, REF MOL4160, IVD, Rx Only, UDI: (01) 20816101027051
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiaSorin Molecular LLC
FDA (openFDA device enforcement)
Reported Oct 27, 2021
P2131 Automated Field Steam Sterilizer NSN: 6530-01-641-4641
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fort Defiance Industries, LLC
FDA (openFDA device enforcement)
Reported Oct 27, 2021
SIGNA Premier nuclear magnetic resonance imaging system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
9 more products in this recall
FDA (openFDA device 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.