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 Mar 11, 2020
RespVent Closed Suction System T-Piece Tracheostomy Adult, Diameter: 4.6mm (14F), Length: 30.5cm (12in.), MDI Adapter,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Respiratory Therapeutics Group LLC
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Elecsys CA 19-9, Cat. No. 07027028190 - Product Usage: the product is an immunoassay for monitoring and management of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seca
FDA (openFDA device enforcement)
Reported Mar 11, 2020
AIA-360 Automated Immunoassay Analyzer, Product Code 019945
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
FDA (openFDA device enforcement)
Reported Mar 11, 2020
Chocolate Fudge Mini Bundt Cake sold by the slice packaged in Self Serve and Plastic clam shell containers PLU 21287
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
3 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 4, 2020
Protective Cover Vivo 55/65 (Used for Vivo 50/65), Part No. 006344. It is an accessory (i.e. protective cover) for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breas Medical, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Selenia Dimensions Mammography System, Model number ASY-04160, Selenia Dimensions Gantry, UDI 15420045505636,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Paleonola Grain Free Granola; The Original; packaged in 10oz stand-up pouches; UPC 013964497144
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Paleonola LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 4, 2020
ADVIA Chemistry Lipase, Ref. No. 01984894 B01-4840-01, Siemens Material No. 10311896, UDI 00630414482446 - Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2020
COHERENCE Oncologist, Model Nos. 07333680 & 07351898
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 4, 2020
Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St Jude Medical, Cardiac Rhythm Management Division
FDA (openFDA device enforcement)
Reported Mar 4, 2020
THP Hip Plating System, Item Nos. 14-451070 14-451075 14-451080 14-451085 14-451090 14-451095 14-451100 14-451105…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2020
SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ormco/Sybronendo
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
CombiDiagnost GCF, Software v. 1.0.5, Product Code 709030 - Product Usage: Xray system, diagnostic, fluoroscopic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems GmbH, DMC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Philips HeartStart FRx AED, Model 861304, FRx codeRev: E.02.017
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2020
Suja Organic Berry Zest Fruit + Veggie Smoothie, 12 oz. UPC: 81861702234
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Suja Life LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Bakers Corner All Purpose Flour in 5 lb. bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Adm Milling
18 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 19, 2020
FlexTip Plus Combined Spinal Epidural Catheterization Set, Product Code AA-05400-B
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
48 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Kushim Tablets (Gushim) 45-count packages, Label in foreign language
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B and a Trading Corporation
FDA (openFDA drug enforcement)
Reported Feb 19, 2020
LivaNova Sorin Connect DPIII KOMPL. S5 REF 96-415-130, 2017-08-15, IPX1, RXOnly, (01)04033817901594 Product Usage: The…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.LivaNova USA Inc.
FDA (openFDA device enforcement)
Reported Feb 19, 2020
bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Market America Inc.
FDA (openFDA food enforcement)
Reported Feb 19, 2020
Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nextremity Solutions
FDA (openFDA device enforcement)
Reported Feb 19, 2020
Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pacific Medical Group Inc.
9 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.