State
73,833 recalls have nationwide distribution and so reach Indiana. 9,598 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,598 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 2,536 (26%) are Severe.
Which agencies issued them
These figures cover only the 9,598 recalls whose distribution notice names Indiana specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Yamaha is recalling about 7,000 model year 2016 YXZ1000R utility vehicles because water in the throttle cable can freeze, preventing the throttle from returning to idle and causing loss of control.
AngioDynamics is recalling 136 NAMIC Convenience Kits because the needle inner lumen is too small to accept the intended 0.038-inch guidewire.
Fresenius Medical Care is recalling 1,650 Hemoflow F3 Dialyzers due to a potential header leak caused by improper torque.
Philips is recalling eValueMed infant heel warmers and transport mattresses because they lack expiration dates and warnings about overheating risks.
AngioDynamics is recalling 100 Renown Regional Medical Center Convenience Kits because the needle inner lumen is too small to accept the intended guidewire.
Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated Systems because a wiring error may leave a module energized when the power cord is unplugged.
AngioDynamics is recalling 45 NAMIC Convenience Kits because the needle inner lumen may be too small to accept a 0.038-inch guidewire.
Immuno-Dynamics, Inc. is recalling PerCoBa Whey Protein Isolate with Colostrum because the labels fail to state that the product contains milk.
Philips is recalling eValueMed Infant Heel Warmers and Transport Mattresses because they lack expiration dates and warnings about overheating risks after shelf life.
Rollerblade USA is recalling about 500 Maxxum inline skating helmets because the plastic shell can crack, causing the helmet to shift and potentially result in head injuries.
Immuno-Dynamics is recalling PerCoBa and Synertek colostrum supplements because the labels fail to state that the products contain milk.
Nitrous Outlet is recalling specific .122 Nitrous Solenoid valves due to improper welding that may cause the piston to eject under pressure, posing an injury risk.
Synthes (USA) Products LLC is recalling specific lots of Titanium Low Profile Neuro Screws because the thread height is undersized, which may affect the device's structural integrity.
Strick Trailers is recalling 460 model year 2004 single axle van trailers because rear impact guard gussets may increase injury risk in crashes.
GE Medical Systems is recalling 16 SIGNA Pioneer MR systems because ferrous material in the Table Control Box could cause unexpected attraction to the magnetic field during servicing, posing a risk of serious injury to personnel.
Focus Diagnostics is recalling Simplexa Direct Amplification Discs because they may cause false test results or error codes.
MicroAire is recalling PAL-R4011XL cannulas because three reports indicated the devices bent or broke during surgical procedures.
AngioDynamics is recalling 8 NAMIC Convenience Kits because the needle inner lumen is too small to accept the intended guidewire.
Applied Medical Resources is recalling specific Epix Universal Clip Applier kits due to a potential loading mechanism nonconformance.
Cardinal Health is recalling Gomco Style Circumcision Clamp Trays because two lots were labeled as containing 1.1cm clamps but actually contained 1.3cm clamps.
Biomet, Inc. is recalling 576 units of Prelude PF Resurfacing Knee System instrumentation due to inadequate design control. The products were distributed to 12 US states.
Siemens Medical Solutions is recalling 49 PACS systems because they may display incorrect distance measurements when used with certain modalities and syngo Imaging.
GE Inspection Technologies is recalling 55 cabinet x-ray systems used for industrial quality control because they may not fully comply with FDA performance standards.
Immuno-Dynamics, Inc. is recalling PerCoBa Colostrum Capsules because the labels failed to state 'contains milk.' The product was distributed nationwide and internationally.
Meditech Laboratories is recalling Formula 3 Injection vials because the active ingredient expired before the labeled Beyond Use Date.