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.
Reported Apr 3, 2013
Siemens Dimension Vista(R) Alkaline Phosphatase (ALP) Calibrator The ALP CAL is an in vitro diagnostic product for the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Siemens Axiom Artis zeego systems with software version VC14, VC20 and VC21 in conjunction with specific technical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Medfusion Model 3500 Syringe Pump, Model #3500-415 and 3500-500. Intended for use in critical care areas for the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD, Inc.
FDA (openFDA device enforcement)
Reported Apr 3, 2013
Synthes Dens Instrument Set (Dens Graphic Case), Part Number 687.030 (also known as the Anterior Column Retractor Set)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
FDA (openFDA device enforcement)
Reported Mar 27, 2013
Extremity Medical - Disposable Orthopedic Surgical Instrument - 1.6 mm Guidewire - Reference Number 101-00006 -…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Extremity Medical LLC
FDA (openFDA device enforcement)
Reported Mar 27, 2013
PrimaConnex Tapered Implant TC, SD Internal Connection 3.5 x 10mm Catalog Number: l5613K. Implants in support for fixed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Elekta Synergy XVI. Radiation Therapy Digital Imager. Product XVI R3.5.1, R4.2.1, and R4.5.1 Used as part of radiation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Genesis Straight Esthetic 4.0 mm 1mm Cuff Abutment Part Number: G71200 Genesis implant for single stage or two stage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Keystone Dental Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 20, 2013
Brilliance 6, 10, 16, 40, 64, Big Bore and the iCT, iCT SP, Ingenuity CT and MX8000 Dual v. EXP are Computed Tomography…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Ad-Tech Medical Instrument Corporation Macro Micro Subdural Electrode. For temporary (<30 days) use with recording,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ad-Tech Medical Instrument Corporation
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Lifeguard Infusion Set with Smartsite, 20Ga, 1, CLGY-2010 Huber type needle set used for the infusion of medical fluids…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Churchill Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Deep Best Quality Dry Garlic Chutney (Thechaa); Net Wt. 4 OZ.; UPC 011433111201; Deep Foods, Inc. Union, NJ 07083
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deep Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 13, 2013
PSX PROXIMATE Skin Staple Extractor, ETHICON ENDO-SURGERY, LLC. For routine skin closure in a wide variety of surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2013
Chocolate bridge mix in 10 oz, 3 oz, and 3.5 oz bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gorant Candies Inc. A Division
3 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 13, 2013
AMSCO C and AMSCO 400 Steam Sterilizers designed for sterilization of heat and moisture-stable materials used in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Steris Corporation
FDA (openFDA device enforcement)
Reported Mar 6, 2013
Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by Philips Medical Systems, Highland Heights, OH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Animas(R) 2020, Animas(R) IR 1250 (1200 plus), Animas(R) IR 1200 Insulin Infusion Pumps Indicated for continuous…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Animas Corporation
FDA (openFDA device enforcement)
Reported Feb 27, 2013
LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell Healthcare Products LLC, Dothan, AL 96303. A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ansell Healthcare Products LLC
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Liko Overhead Rail System, Ceiling Mounted Rail Systems for all Liko Stationary Lifts including Likorall, Multirall and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hill-Rom, Inc.
FDA (openFDA device enforcement)
Reported Feb 27, 2013
Vascular Solutions, SuperCross Microcatheter, Sterilized using ethylene oxide, Rx Only, Model numbers 5300 - 5307,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Feb 20, 2013
The Lumenis VersaCut Tissue Morcellator Product Usage: is intended for use under direct or endoscopic visualization for…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lumenis Limited
FDA (openFDA device enforcement)
Reported Feb 20, 2013
Mizuho Orthopedic Table, model 5855, sub assembly 5855-901 Orthopedic Table Spar.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mizuho OSI
FDA (openFDA device enforcement)
Reported Feb 20, 2013
St. Jude Medical, AGA Medical corporation, AMPLATZER¿ TorqVue¿ FX Delivery System. Model #'s: 9-ITVFX06F45/60,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.St Jude Medical Inc.
FDA (openFDA device enforcement)
Reported Feb 13, 2013
Synthes(R) Spine Vectra, Vectra-T and Vectra-One Anterior Cervical Plating for Spinal Fusion - 2.5mm Drill Bit,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes USA HQ, Inc.
1 more product 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.