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 Jun 29, 2016

Dakota Style Roasted & Salted Sunflower Kernels, Net Wt. 3.5 oz. plastic bag. UPC 84872-20172

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

Dakota Style, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jun 22, 2016

The XN-Series modules (XN-10, XN-20) are quantitative multi-parameter automated hematology analyzers intended for in…

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

Sysmex Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jun 15, 2016

Ellipse ND: YAG Laser applicator for Ellipse Multiflex Medical Laser Products.

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

Ellipse A/S

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Jun 15, 2016

Nuvi Global StemVitae Multivitamin 30oz.

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

Nuvi Global Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jun 15, 2016

Sedecal SA Mobile Diagnost w DR x-ray system

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

Sedecal USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic steroid, in plasma.

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

Abbott Laboratories

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…

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

B. Braun Medical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Monaco RTP System Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Replacement HEPA filter for Natus Sterile-Drier Model 43 and Model 44. Filter Catalogue Part Number: 54343, 54344, and…

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

Natus Medical Incorporated

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Firebird NXG Spinal Fixation System Set Screw Driver used to insert a set screw into a spinal fixation construct. Rx…

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

Orthofix, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body…

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

Philips Medical Systems (Cleveland) Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 8, 2016

Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…

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

Siemens Healthcare Diagnostics Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jun 1, 2016

GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.

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

GE Medical Systems, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 25, 2016

Bunge Soy Clear Fry Oil OU, 35 lb., Manufactured by: Bunge Oils, Inc. Kearny, NJ 07032, UPC 00078684692026

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

Bunge Oil North America Inc.

23 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 25, 2016

Diamedix Is-Mumps IgG Test Kit Diamedix Is-Mumps IgG Test Kit is an EIA procedure intended for the qualitative and…

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

Diamedix Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…

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

Applied Medical Resources Corp.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Arctic Sun Temperature Management System, 5000, 100-120V and 220-240V The product is a thermal regulating system…

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

C.R. Bard, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 18, 2016

Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient Monitor, Battery Packs Model Number - 016400,…

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

Medtronic

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 11, 2016

TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC STAYS STERILE EO Rx ONLY Product Usage:…

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

Applied Medical Technology Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 11, 2016

Classic Creme Cookies, Net wt. 12 oz cartons, 6 cartons per case. Manufactured for Back To Nature Foods Co., LLC

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

Back To Nature Foods, LLC

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2016

BD Trucount Absolute Counting Tubes: Model number: 340334 IVD; BD Trucount tubes are used for determining absolute…

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Food

Reported May 4, 2016

Bliss French Vanilla Ice Cream 64oz Product Code: 51051

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

Bliss Bros Dairy, Inc.

21 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 4, 2016

ev3, PowerCross" 0.018" OTW PTA Dilatation Catheter, model: AB18W030200150, Sterile EO, Rx Only.

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

ev3, Inc.

FDA (openFDA device enforcement)

Food

Reported May 4, 2016

Family Gourmet Long Grain Enriched White Rice, 32 oz. (2 lb.) plastic bag (SKU: 1218898)

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

Family Dollar Stores - NC Distribution Center

1 more product in this recall

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.