State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Cantrell Drug Company is recalling 87 bags of Ropivacaine HCl 0.25% due to a lack of assurance of sterility. The product is intended for epidural use only.
Becton Dickinson is recalling specific lots of BD Vacutainer Push Button Blood Collection Sets because the front and rear barrels may separate when the safety feature is activated.
Inovo, Inc. is recalling 117 Inovo Purefill Oxygen Compressor Model PF1100 units because the device can fail during operation.
Steris Corporation is recalling 63 Harmony Insight Diagnostic Monitor Support Systems because spring arm screws may not be properly secured and could become loose.
Stryker is recalling 40,476 reprocessed Xcel Bladeless Trocars because the adjustable plug may break in packaging or during use.
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflator initiators may fail to ignite during a crash, preventing deployment.
Toyota is recalling 2017 86 vehicles with automatic transmissions and ignition keys because the key may be removed without the transmission in Park, increasing the risk of the vehicle rolling away.
Bluecar is recalling 235 2016 vehicles because water may leak into the high voltage connector in heavy rain or snow, potentially causing the engine to shut down.
Toyota is recalling one 2016 4Runner and one 2017 Lexus GX460 because the front passenger air bag may not fully inflate in a crash.
Teleflex Medical is recalling 2,265 units of Weck Facial Closure Systems because the device wings may partially detach from the shield during use.
Teleflex Medical is recalling Visistat 35W disposable skin staplers because improper packaging seals mean sterility is not assured.
Prism Medical is recalling carry bars for patient lifts because a black plastic puck may break, posing a risk of harm to patients.
Encore Medical is recalling 162 Empowr PS Knee System Box Cut Guides because femoral chipping occurred during surgery.
Elekta is recalling 47 MOSAIQ Oncology Information System units because edits to particle field definition parameters may not be saved.
Stryker is voluntarily recalling 749 Performance-LOAD Ambulance Cot Fasteners because they may not fasten securely, posing a risk of injury.
Giant Eagle is recalling 248 units of Farmers Market Buffalo Hot Peanuts because they contain undeclared cashews and wheat. The error was caused by mislabeling at the manufacturer.
Merge Healthcare is recalling Merge Cardio software versions 8.30.0 through 10.1.1 because images sent without an order may be matched to the wrong accession number.
Cargill is recalling Crisco Professional Liquid Butter Alternative because it contains excessive amounts of TBHQ and DMPS. The product was distributed to 29 states.
GE Healthcare is recalling specific Avance CS2, Avance, and Amingo anesthesia devices because they may enter a System Malfunction state if a storage drawer closes with excessive force.
GF Health Products is voluntarily correcting Patriot homecare beds because contaminated motor housings may crack, potentially causing the head section to fall.
Natus Medical is recalling neoBLUE blanket LED Phototherapy Systems due to discoloration and degradation of the fiberoptic bundle at the pad and box connection.
Merge Healthcare is recalling Merge Cardio software versions 10.1 and 10.1.1 because the reporting feature times out after one hour of inactivity, causing data loss.
Halyard Health is recalling Sterling Nitrile Sterile Powder Free Exam Gloves because they may be discolored and brittle, causing them to tear when put on.
Cargill is recalling 1-gallon bottles of refyne Butter Flavored Oil because they contain excessive amounts of TBHQ and dimethyl polysiloxane.
Siemens is recalling 104 SOMATOM Definition Flash CT systems to install a software and firmware update that fixes bugs and improves performance.