State
73,809 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Boston Scientific is recalling PROPONENT EL DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Consumers should check for discoloration on the protective seal.
Boston Scientific is recalling ALTRUA 2 DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Pharmedium Services is recalling 5,002 pre-filled ephedrine sulfate syringes nationwide because the drug was subpotent. The voluntary recall was initiated in October 2017.
Fashion Accessory Bazaar is recalling Pokemon fidget spinner keychains because the center post can fall out, posing a choking hazard. No injuries have been reported.
Hetero Labs is recalling specific lots of Simvastatin 40 mg tablets because a metallic razor blade was found in one bottle.
Boston Scientific is recalling ESSENTIO MRI EL DR Pacemakers because reports indicate the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling ESSENTIO MRI DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling ESSENTIO SR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Phadia US Inc is recalling 70 Phadia 1000 Instruments nationwide because a malfunctioning Retry command may cause solution shortages and affect test results.
Boston Scientific is recalling ACCOLADE DR pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Ventura Foods is recalling A&W Papa Sauce because a plastic foreign object was inadvertently introduced into the product stream.
Boston Scientific is recalling ACCOLADE EL DR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling ACCOLADE MRI DR Pacemakers because reports indicate the Minute Ventilation sensor may intermittently over-sense signals.
Boston Scientific is recalling PROPONENT DR Pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Dainese is recalling 325 AGV Carbon Modular motorcycle helmets because glue may have caused the chin base material to deteriorate, increasing injury risk.
Boston Scientific is recalling ACCOLADE SR pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling VALITUDE CRT-P pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling PROPONENT MRI Pacemakers because of reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling VALITUDE X4 CRT-P pacemakers due to reports of intermittent over-sensing of the Minute Ventilation sensor signal.
Boston Scientific is recalling ALTRUA 2 SR pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Owen Mumford USA is recalling Unifine Pentips pen needles because water exposure may have compromised sterility. Users should check for discoloration or yellowing of the protective seal.
Boston Scientific is recalling VISIONIST X4 CRT-P Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.
Unichem Pharmaceuticals is recalling Divalproex Sodium tablets because metronidazole powder was found in one bottle. The product was distributed nationwide.
Boston Scientific is recalling ALTRUA 2 EL DR Pacemakers because the Minute Ventilation sensor may intermittently over-sense signals.