State
73,722 recalls have nationwide distribution and so reach Indiana. 9,596 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,596 recalls naming Indiana we have scored against our rubric, 1,908 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,534 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,596 recalls whose distribution notice names Indiana specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wellspect HealthCare is voluntarily recalling specific LoFric Origo urinary catheters because of a potential defect in the distal tip.
Carefusion 2200 Inc is recalling Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling IcePearl 2.0 CX 90 Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Medtronic Xomed is recalling IPC software upgrade v 2.7.3.0 because the M5 Microdebrider may rotate faster than the set value.
REV Recreation Group is recalling 2019-2020 Fleetwood Pace Arrow motorhomes because loose battery brackets may cause a short circuit and fire.
Carefusion 2200 Inc is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Safe-T 8 Fr Thora-Para Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion is recalling Safe-T PLUS Thora-Para 5 Fr Non-Valved Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 79 IceFORCE 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
Boston Scientific is recalling 88 Prostate Cryoablation Kits because needle surfaces deteriorated during procedures due to unexpected electrolysis.
Carefusion 2200 Inc is recalling Safe-T 5 Fr Thora-Para Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Safe-T-Centesis PLUS 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Safe-T-Centesis PLUS 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 193 IcePearl 2.1 CX Prostate Kits because needle surfaces deteriorated due to unexpected electrolysis during procedures.
Boston Scientific is recalling 205 IcePearl 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Philips is recalling 3,075 IntelliVue G7m Anesthesia Gas Modules due to a firmware issue that may interrupt gas measurement and display.
EHOB, Inc. is recalling 173 Expansion Control Overlays (Item No. 1004EC) because a portion of the lot may have been contaminated with blood.
Carefusion 2200 Inc is recalling Safe-T PLUS Thora-Para 8 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Carefusion 2200 Inc is recalling Thora-Para 5 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Boston Scientific is recalling 39 IceFORCE 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Boston Scientific is recalling 656 IceForce 2.1 CX Cryoablation Needles because the needle surface deteriorated due to unexpected electrolysis during procedures.
Wellspect HealthCare is voluntarily recalling LoFric Origo urinary catheters due to a potential defect in the distal tip.
BMW is recalling 2020 X3 vehicles because they lack rearview camera software, increasing crash risk when reversing.
Carefusion 2200 Inc is recalling Safe-T-Centesis 6 Fr Catheter Drainage Trays because internal valve leaks may introduce up to 30cc of air into patients.
Sysmex America, Inc. is recalling eight PS-10 Sample Preparation Systems because they may contain insufficient antibody without triggering an error message or alarm.