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.
2,040 stored notices name New Hampshire, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,784 notices were distributed nationwide, so they reach New Hampshire too — those are in the archive.
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
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)
Reported May 4, 2016
Dunkin Donuts Brand Italian Sub, Net Wt 7.7 oz packaged in Bag, Clear View
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Flying Food Group LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported May 4, 2016
RESTORIS PST RIO Offset Shell Impactor For use by orthopedic surgeons specifically for the purpose of positioning and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported May 4, 2016
Andrographis extract 400 mg packaged in a white and orange bottle containing 90 capsules. The bottle has a blue cap and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NOW Foods
4 more products in this recall
FDA (openFDA food enforcement)
Reported May 4, 2016
SOMATOM Force, Computed Tomography x-ray system intended to generate and process cross-sectional images of patients by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported May 4, 2016
Pleur-evac Chest Drainage System, Dry Suction/Dry Seal Control, REF A-6000-08LF, Rx Only, Teleflex Medical. Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported May 4, 2016
The Super Elixir By WelleCo Australia Alkalising Greens 150g/5.3 oz net, 300g/10.6 oz net Fine Powder welleco.com
High riskUsing this product could cause serious injury, illness or death — stop using it now.Welle Pty Ltd.
FDA (openFDA food enforcement)
Reported Apr 29, 2016
Greencore USA Retira Productos de Carne De Res Y Pollo Producidos Sin El Beneficio De Una Inspeccion Federal
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
Reported Apr 27, 2016
Acorn 180 Curved Stairlift
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acorn Stairlifts Inc.
FDA (openFDA device enforcement)
Reported Apr 27, 2016
GoGo squeeZ, non-organic Apple Sauce pouches, 3.2 oz., 12 x4, 6 x12, 1 x 18, 1 x 48, 1 x100, 36 x 4, Mighty Mango Fruit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Materne North America Corp.
16 more products in this recall
FDA (openFDA food 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.