State
73,824 recalls have nationwide distribution and so reach New Hampshire. 4,483 additional recalls listed New Hampshire specifically in their distribution scope.
Of the 4,483 recalls naming New Hampshire we have scored against our rubric, 603 (13%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,049 (23%) are Severe.
Which agencies issued them
These figures cover only the 4,483 recalls whose distribution notice names New Hampshire specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling 4,500 EMBLEM S-ICD Programmer Model 3200 units due to a potential risk of radio frequency interference causing unintended commands during in-clinic sessions.
Physio-Control is recalling LIFEPAK 15 Monitor/Defibrillators with End-Tidal CO2 options because the CO2 reading may intermittently display an incorrect value of XXX.
Stryker Leibinger is recalling QUINTUBE Monitor Packs and SPG Bulb Drain Systems because non-sterile products were incorrectly labeled as sterile.
Merge Healthcare is recalling 182 Eye Station capture stations because they may fail to capture eye images as intended, posing a risk to patient health.
Physio-Control is recalling LIFEPAK 12 Defibrillators because the End-Tidal CO2 reading may intermittently display an invalid value of XXX during operation.
Stryker Leibinger is recalling specific non-sterile Medpor implant sizer sets because they were incorrectly labeled as sterile. The recall covers 619 units distributed in the US and several international countries.
VistaPharm is recalling 13,609 cases of Potassium Chloride Oral Solution because the unit dose cups may leak at the seal.
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Ammonia Flex reagent cartridges because they may not meet the 60-day calibration interval claim, potentially leading to abnormal assay results.
Siemens is recalling specific lots of Dimension Vista Ammonia Flex reagent cartridges because they may not meet the 60-day calibration interval claim, potentially resulting in abnormal assay results.
Ortho-Clinical Diagnostics is recalling VITROS FS Calibrator 1, Lot 91461, because it cannot calibrate dLDL reagents when used with specific Assay Data Disk versions.
Encore Medical is recalling 24 Empowr PS Knee Tibial Inserts because they are missing the impaction slot feature.
Ortho-Clinical Diagnostics is recalling VITROS UPRO Slides because they may produce variable urine protein results.
Thayer Medical Corporation is recalling 2,550 MiniSpacer MDI adapters because the insert and case labels incorrectly state the connection size.
Aurobindo Pharma USA Inc is recalling 29,800 vials of Pantoprazole Sodium for Injection due to discoloration. The affected vials contain powder with a yellowish-brownish appearance.
Dr. Reddy's Laboratories is recalling Olanzapine tablets because an impurity exceeded specification limits during stability testing.
Apotex Inc. is recalling 67,946 bottles of 2 mg Aripiprazole tablets because the product may not meet specifications throughout its shelf life.
Chrysler is recalling 2014-2017 Dodge Charger and Chrysler 300 AWD vehicles because front driveshaft bolts may loosen, potentially causing a loss of motive power and increasing crash risk.
Foretravel is recalling 2015-2017 Realm motorhomes because restricted brake pedal movement may prevent full braking, increasing crash risk.
Gillig is recalling 2,787 Low Floor transit buses because front LED turn signals may not be visible enough to other drivers or pedestrians.
Thor Motor Coach is recalling 2,483 motorhomes because improperly installed windshield wipers may fail, reducing visibility and increasing crash risk.
Forest River is recalling 2017 Palomino Columbus recreational vehicles equipped with an optional generator package because the liquid propane supply hose may be too small, posing a fire or explosion risk.
Target is recalling about 1,300 Threshold patio benches because they can collapse while in use, posing a fall hazard.
Daimler Vans USA is recalling 2015 Mercedes-Benz Sprinter 2500 and 3500 vehicles because missing protective parts may allow fuel leaks and fire risks.
Daimler Vans USA is recalling 2013-2016 Sprinter vans because the air bag control unit may fail to function after a first impact, increasing injury risk.
Daimler Vans USA is recalling 2015 Mercedes-Benz Sprinter 2500 and 3500 vehicles because a missing driveshaft catch strap could allow the driveshaft to strike the fuel tank, increasing fire risk.