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 Jan 28, 2015
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Jan 28, 2015
PF4 Concentrated Wash (10x), REF 403624, packaged in the following assay kits: 1. ImmucorGamma LIFECODES PF4 IgG…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Genetic Testing Institute,Inc.
FDA (openFDA device enforcement)
Reported Jan 21, 2015
iPlan RT Dose is a stereotactic radiation treatment planning system that is intended for use in stereotactic,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 21, 2015
Femto LDV Z-Generation Femtosecond Surgical Lasers are used to perform ophthalmic surgeries.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ziemer USA Inc.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Abdallah Milk Chocolate Bites CARAMEL, Net Wt 4.5 oz. (127g), UPC 7 6668407116 2, Ingredients: Pure milk chocolate…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Abdallah Candies, Inc.
FDA (openFDA food enforcement)
Reported Jan 14, 2015
McKesson Cardiology ECG Management It is a software application designed to import, display, store, analyze, distribute…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Israel Ltd.
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Cable remote control JUPITER U, Material no.4500119, Serial number: to (incl.) 102306915. Patient positioning during…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trumpf Medical Systems, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 14, 2015
Vintage Pure Bee Flower Honey, Net Weight 16.4 oz (465g), Packaged in a Glass Jar, Product of Turkey, Imported by:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Vintage Food Corp.
FDA (openFDA food enforcement)
Reported Jan 7, 2015
Organic Cilantro Medium Bulk - size is dependent on customer request; Certified Organic by QAI High Quality Organics…
High riskUsing this product could cause serious injury, illness or death — stop using it now.High Quality Organics, Inc.
FDA (openFDA food enforcement)
Reported Dec 31, 2014
Bausch & Lomb Stellaris PC w/ Laser, BL14304 The responsible firm name is Bausch & Lomb Incorporated Rochester, NY
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 31, 2014
KimVent Microcuff Subglottic Suctioning, Endotracheal Tube, 7.0 mm, Distributed by Kimberly Clark Global Sales, LLC.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Halyard Health
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Radiomat M+ NIF 14 x 17, Radiomat M+ NIF 35CM x 43CM, Radiomat M+ NIF 10 x 12, Radiomat M+ NIF 25,4CM x 30,5CM
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.AGFA Healthcare Corp.
FDA (openFDA device enforcement)
Reported Dec 24, 2014
GE Cabinet X-ray systems
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Inspection Technologies, LP
FDA (openFDA device enforcement)
Reported Dec 24, 2014
Dark Cocoa Sorbetto packed in 14 oz. plastic jars, 8 packages per case, manufactured from 4/11/14-4/12/14; product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.House Of Flavors, Inc.
FDA (openFDA food enforcement)
Reported Dec 24, 2014
RESTORIS PST Straight Shell Inserter An impactor is a reusable instrument designed for use by orthopedic surgeons…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Invacare Perfecto 2 V Oxygen Concentrator The finished device is packaged as a single unit. The service part contains a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Dec 17, 2014
Chicken flavored broth base and seasoning, low sodium sold under the Orrington Farms brand in 5 oz. plastic jars.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kent Precision Foods Group, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2014
ESSENTIA Hydration Perfected Purified Water and Electrolytes, 9.5 pH, Manufactured for Essentia Water Inc., 22833…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nature's Way Purewater Systems, Inc.
FDA (openFDA food enforcement)
Reported Dec 17, 2014
Crocodile (size 3) are two-armed, wheeled walking aids, used by children with disabilities. Product Usage: The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Snug Seat Inc.
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Amerigel Hydrogel Wound Dressing Wound management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amerx Health Care Corp.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
GDC-10 360 SOFT 3mm x 6cm SR ; GDC 360¿ Detachable Coils are intended for embolization of those intracranial aneurysms…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 10, 2014
Aquapak Adaptor, 028 NEB, INTL, Product No. 403128; Aquapak Adaptor, 033 NEB, INTL, Product No. 403133; Aqaupak…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Calcitonin ELISA Kit, Code No. 7024, 7024BU. Intended use of this product is the quantitative determination of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerica
FDA (openFDA device enforcement)
Reported Dec 3, 2014
Trabecular Metal Tibial Impactor. Product Usage: TM Tibial Impactor pads are used in conjunction with the TM Tibial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, 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.