All recall categories

Recalls distributed in New Hampshire

These notices name New Hampshire 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.

2,001 stored notices name New Hampshire, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach New Hampshire too — those are in the archive.

Food

Reported Mar 6, 2019

Mediterranean Stuffed Salmon packaged in plastic nonflexible containers

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Whole Foods Market

33 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 27, 2019

AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 27, 2019

Snak Club Praline Pecans Made With Cane Sugar NET Wt. 2.25 oz (64 g) Produced By: Century Snack Commerce, CA 90040…

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

Century Snacks LLC

FDA (openFDA food enforcement)

Meat & poultry

Reported Feb 26, 2019

Sahlen Packing Company, Inc. Recalls Ready-To-Eat Deli Meat Products Due to Possible Foreign Matter Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Sahlen Packing Company, Inc.

USDA FSIS

Medical devices

Reported Feb 20, 2019

COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002

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

AtriCure, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton

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

Chicago Bar Company LLC Rxbar

18 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 20, 2019

Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Diamond Crystal Brands, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Organic Sunflower Butter, Net Wt. 16 oz. (453g) Packaged under the following brand names: 1. Thrive Market, UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Oskri Corp.

19 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 20, 2019

Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year…

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

PBM Nutritionals, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Feb 13, 2019

Henry Schein CU 1000 Halogen Curing Light, Catalog 900-4542. - Product Usage: Curing light for use in dentistry. The…

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

Handpiece Headquarters

FDA (openFDA device enforcement)

Medical devices

Reported Feb 13, 2019

Portex 350 ml Sterile Water Humidifier w/5psi Adapt.¿¿¿¿

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company

12 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 6, 2019

Cell Saver 5/5+ Bowl Set, 70ml, Product ID: 0291E-00, 0291A-00 Indications for Use: The Haemonetics Cell Saver 5/5+…

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

Haemonetics Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 30, 2019

Del Monte Quality Fresh Cut Harvest Selects Fiesta Corn seasoned with Red & Green Peppers. NET WT 15.25 oz. (432 g);…

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

Del Monte Research Center - Walnut Creek

FDA (openFDA food enforcement)

Medical devices

Reported Jan 30, 2019

Perfusion Pack, Rx only, Sterile EO

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

LivaNova USA

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

Arthrex Suture Anchor, Nano Corkscrew FT (consists of an anchor pre-loaded on a handled inserter including suture, with…

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

Arthrex, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 23, 2019

U by Kotex¿ Sleek¿, Regular Tampons, 18 Count

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

Kimberly-Clark Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 16, 2019

Various GE Magnetic Resonance System on-site software version Product Usage: Magnetic resonance imaging equipment for…

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

GE Healthcare, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

StealthStation Cranial and Synergy Cranial Depth Gauge: StealthStation Cranial Optical Pocket Guide - Instructions for…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 9, 2019

Enamelast Cool Mint/OT Varnish 5% NaF Mint Label Enamelast Unit Dose 200pk Cool Mint: Enamelast 5% Sodium Fluoride Unit…

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

Ultradent Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

HydroSet XT Injectable HA Bone Cement, REF 897003, STERILE

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

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 2, 2019

Medtronic MiniMed 630G 6025805-003_C, Rx Only Medtronic MiniMed 670G 6025805-005_B, Rx Only Medtronic MiniMed 640G…

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

Medtronic Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 2, 2019

Sea Salt Caramels Tumbled In Milk Chocolate, Moonstruck brand. The product sold in an individual resealable plastic…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Moonstruck Chocolate Company

FDA (openFDA food enforcement)

Medical devices

Reported Dec 26, 2018

enVista One Piece Hydrophobic Acrylic Intraocular lens - Is indicated for primary implantation for the visual…

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

Bausch & Lomb Surgical, Inc.

FDA (openFDA device 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.