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 Mar 12, 2014
All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version 5.4, 5.5, or 5.6 with the Automatic-View-On-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 12, 2014
Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's Robotic Arm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Kinnikinnick Pancake & Waffle Mix -Weight: 454g/16 oz Cardboard Box UPC 62013310512 2
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bozzutos' Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 5, 2014
GE Healthcare - Giraffe Warmer;Panda Warmer;Panda iRes Warmer, Giraffe Stand-alone Infant Resuscitation System. Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.GE Healthcare, LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Medtronic Everest 20cc Inflation Device; Model Number and Catalog Number: AC2205P The Everest 20cc Inflation device is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Medtronic Vascular
FDA (openFDA device enforcement)
Reported Mar 5, 2014
VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
HeartStart MRx Monitor/Defibrillator; Model(s), Catalogue, or Code Number: M3535A, M3536A, M3536J, M3536MC The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 5, 2014
pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Mar 5, 2014
Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smith & Nephew Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2014
Synergy XVI XVI can incorrectly calculate the target position of the treatment table, because of an error that does not…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 26, 2014
Merit Medical's Custom Procedural Trays or Kits containing 1% Lidocaine HCl Injection, USP, 10 mg/mL, Lot 25-090-DK.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Feb 26, 2014
Digestive enzyme capsules sold under the NOW Foods, Beeyoutiful, Best in Nature, Bluegrass Naturals Vitamin Company,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NOW Foods
FDA (openFDA food enforcement)
Reported Feb 19, 2014
The UF-1000i is a fully automated urine particle analyzer intended for vitro diagnostic use in urinalysis. The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sysmex America, Inc.
FDA (openFDA device enforcement)
Reported Feb 5, 2014
Walmart Great Value Tex Mex Trail Mix, Net Wt 28 oz (793g), Distributed by Wal Mart Stores, Inc., Bentonville, AR,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ann's House
FDA (openFDA food enforcement)
Reported Jan 29, 2014
ABL90 FLEX Analyzer Radiometer Medical ApS, ¿kandevej 21 Br¿nsh¿j, Denmark A portable, automated analyzer that measures…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Locking Cortical Screw 3.5mmX38mm REF 8161-35-038
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Draeger Infinity Acute Care System Monitoring Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Draeger Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Centricity PACS System versions 3.X and higher and 4.X and higher Product Usage: The Centricity PACS Workstation is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ge Healthcare It
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 22, 2014
Leica BIOSYSTEMS; BOND Polymer Refine Red Detection; Catalog No: DS9390; Leica Biosystems Newcastle Ltd; Balliol…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Newcastle Ltd.
FDA (openFDA device enforcement)
Reported Jan 15, 2014
SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed As GE Healthcare CARESCAPE Patient Data Module)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Jan 15, 2014
NanoClave Connector, Part No. A1000, Item No. 011-A1000, 061-A1000, A1000, K7083-001, Z3769 The ICU Needleless…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
49 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
Integra Small Rickham -Style Reservoir Rx Only Sterile for Single Use Only Integra NeuroSciences 311 Enterprise Drive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jan 15, 2014
The Vantage Digital Panoramic System delivers high-value features standard on every system: - Five pre-programmed exam…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Midmark Corp. dba Progeny Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new New Hampshire recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.