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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.

Food

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)

Medical devices

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

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)

Food

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)

Medical devices

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)

Drugs

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)

Medical devices

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)

Food

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)

Medical devices

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)

Medical devices

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)

Medical devices

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)

Food

Reported Feb 19, 2020

Ready Pac Bistro - Spinach Dijon Salad with Sweet Onion Dijon Vinaigrette; Baby Spinach, Hard Boiled Eggs, Monterey…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Ready Pac Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

cobas infinity core, Material No. 7154003001. The device is a calculator/data processing module, for clinical use.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Granulate Pure Cane Sugar sold under the brand names of: Ahold 16 oz canister, DISTRIBUTED BY FOODHOLD USA, LLC,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Sugar Foods Corporation

FDA (openFDA food enforcement)

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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.