State
73,817 recalls have nationwide distribution and so reach American Samoa. 25 additional recalls listed American Samoa specifically in their distribution scope.
Of the 25 recalls naming American Samoa we have scored against our rubric, 1 (4%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 9 (36%) are Severe.
Which agencies issued them
These figures cover only the 25 recalls whose distribution notice names American Samoa specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Hale Products Inc. is recalling Fire Pump Engagement Pressure Switches that may fail in extremely cold temperatures, potentially delaying water delivery during fires.
Volvo is recalling 2017 XC90, S90, and V90 Cross Country vehicles because side air bag bolts may break, causing improper deployment in a crash.
PACCAR is recalling 2015-2018 Kenworth and 2017-2018 Peterbilt trucks because plastic fuel tee fittings may leak fuel, increasing the risk of fire.
Blue Bird is recalling 2015-2018 Vision school buses because battery box brackets may crack, causing the box to detach and become a road hazard.
Prevost is recalling 2017 H3-45 and X3-45 motor coaches because incorrectly forged steering arm levers may crack and fail, increasing crash risk.
Carestream Health is recalling DRX-Revolution Mobile X-Ray Systems because a complaint alleged the unit could not be stopped when applying the brake, resulting in a crash into an elevator.
Blue Bird is recalling 2015-2018 Vision transit buses because battery box brackets may crack, causing the box to detach and create a road hazard.
Bayer is recalling Medrad Intego PET Infusion System pumps because the administration sets may produce particulates in radiopharmaceutical vials.
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.
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.