State
73,104 recalls have nationwide distribution and so reach Indiana. 9,585 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,585 recalls naming Indiana we have scored against our rubric, 1,913 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,148 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,585 recalls whose distribution notice names Indiana specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medartis Inc. is recalling APTUS 2.8 TriLock Screws (lot 24377397) because some units are 16mm long instead of the specified 22mm, which could compromise bone fixation stability.
Andover Healthcare Inc. is recalling CoFlex NL sterile flexible cohesive bandages (model 5400S) due to packaging seal gaps that could compromise product sterility. No illnesses have been reported.
Cardinal Health is recalling Curity Flexible Adhesive Bandages (Model 44102, Lot #A14722) due to potential contamination with latex adhesive residual. The hypoallergenic product was distributed nationwide to approximately 2,000 packages.
TriMed Inc. is recalling 142 units of Threaded IM Nails with an out-of-specification driver-socket that could prevent proper surgical nail fixation and torque application.
ST Engineering Hackney is recalling 2023-2024 Kidron Refrigerated Trailers because wheel lug nuts may not be tightened properly, increasing the risk of a crash.
Philips Ingenia 1.5T MRI systems with software R5.7.1 may not provide adequate warning for low ventilation conditions, potentially causing increased patient body temperature or burning sensation.
Maquet Medical Systems USA is recalling the CARDIOHELP-i System because measured patient leakage current in some units significantly exceeded expected safety levels.
Fisher & Paykel's Airvo 2 and myAirvo 2 respiratory humidifiers have a speaker defect that may silence or distort critical alarm sounds. If the alarm fails and therapy is interrupted, patients could experience oxygen desaturation.
Fresenius is recalling 88 Novalung sensor boxes for error messages affecting flow measurement. The defect impacts measurement capabilities in a life-support system used for acute respiratory and cardiac failure patients.
Certain HeartSine PAD defibrillators may fail to deliver voice prompts during emergency use due to a manufacturing defect, potentially delaying therapy. Visual instructions remain available.
Volkswagen is recalling certain 2022-2024 Audi Q4 e-tron and Q4 e-tron Sportback vehicles because incorrect headlight control module software may have been installed, failing FMVSS 108.
Macherey Nagel urinalysis test strips are recalled due to a missing leukocytes test pad on some packages, potentially resulting in false negative results for urinary tract infections and renal inflammation. Affected lot: 65402.
Sophysa is recalling the Pressio Ventricular Intracranial Pressure Monitoring Kit due to manufacturing defects causing cerebrospinal fluid leakage from the catheter. Undetected leaks during implantation could result in infection risk to patients.
Ossur RHEO KNEE prosthetic units recalled due to firmware issues causing unintended warnings and device shutdown, which could result in patient falls.
TriMed Threaded IM Nail 3.6mm implants are being recalled due to a driver-socket defect that could prevent proper nail pickup or torque application. The recall affects 120 units from lot QM23087 distributed nationwide.
Karl Storz laser surgical instruments lack validated sterilization procedures, creating infection risk after reprocessing. The FDA has recalled 85 units distributed nationwide and in Argentina.
East West Tea Company is recalling Organic Yogi Echinacea Immune Support tea bags nationwide due to pesticide residues detected above FDA action levels.
Meijer Magnesium Citrate Saline Laxative is being recalled due to microbial contamination. Lot A81834 (expiration 1/31/2026) was distributed nationwide; consumers should stop using the product.
Gordofilm Wart Remover by Gordon Laboratories is being recalled nationwide due to Current Good Manufacturing Practice (cGMP) deviations. The FDA classified this as a Class II recall on May 13, 2024.
CVS Health Magnesium Citrate Saline Laxative Oral Solution is being recalled nationwide due to microbial contamination with Acetobacter nitrogenifigens bacteria in lot A81506.
Kia is recalling 2022 Niro EV vehicles because a high-voltage battery safety plug may overheat and melt, potentially causing a fire or loss of drive power.
Cummins is recalling L9 diesel engines because remote fuel filter hoses may separate, causing fuel leaks, fire risks, or engine stalls.
Turtle Top is recalling 2024 Van Terra, Terra Transit, Odyssey, and Odyssey XL vehicles because the seat recliner mechanism may not engage, increasing injury risk in a crash.
Prime-Time is recalling 2023-2024 Ford Transit conversions because the seat recliner mechanism may not engage, increasing injury risk in a crash.
Vermeer is recalling 2015-2022 BC900XL brush chipper trailers because the service manuals list incorrect lug nut torque values, which could lead to wheel detachment.