State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Mederi Therapeutics is recalling 1,458 Stretta Catheter kits because a breach in the sterile barrier package compromised sterility.
Isuzu is recalling certain 2008-2009 and 2012-2013 NPR, NPR HD, and GMC W3500/W4500 trucks because the throttle pedal may get stuck, causing high speeds and crash risk.
Zimmer Biomet is recalling 8,154 Regenerex Series A Patella implants because the pegs may shear after surgery.
Frito-Lay is recalling 12-count Lays Kettle Cooked Multipacks nationwide due to potential Salmonella presence.
Arthrex, Inc. is recalling specific Anthrex PEEK SwiveLock SP Vented anchors because some eyelets broke during insertion.
Stryker is recalling 119 Medi-Therm Hyper/Hypothermia Systems because the water may reheat too quickly under specific operating conditions.
Roche Diagnostics is recalling 3,946 sample probes for cobas analyzers because corrosion on electrical contacts can disrupt liquid level detection, potentially causing sample carryover.
Teva Pharmaceuticals is recalling specific lots of Clozapine Tablets USP, 25 mg, due to microbial contamination of non-sterile products.
Pinnacle Foods is recalling Great Value Bread and Butter Chips because glass fragments were found in the product. The chips were distributed nationwide.
Arthrex, Inc. is recalling the Anthrex SpeedBridge Implant System because some eyelets broke from the SwiveLock Anchor during insertion.
Treehouse Foods is recalling specific brands of microwaveable macaroni and cheese cups because they may be contaminated with Salmonella.
Douglas is recalling Oliver, Chewie, and Charlotte plush toys because plastic eyes can detach, posing a choking hazard to young children.
Bison Coach is recalling 2016-2018 horse trailers due to incorrect Gross Axle Weight Rating labels, which may lead to overloading and increased crash risk.
Cabrinha is recalling about 2,900 kiteboard control systems because a stainless steel component can break, causing loss of kite control and posing injury and fall hazards.
Arthrex, Inc. is recalling specific Bio-SwiveLock SP Vented anchors because some eyelets broke during insertion.
Arthrex is recalling specific batches of Bio Composite SwiveLock anchors because some eyelets broke during insertion.
Siemens is recalling 159 RAPIDPoint 500 Blood Gas Analyzers because a blank patient ID field may cause demographic errors.
PAR Sterile Products LLC is recalling Buprenorphine Hydrochloride Injection due to the presence of white, crystalline particulates in the vials.
Zimmer CAS is recalling 34 NDI P7 Position Sensors due to a manufacturing issue that may cause them to stop functioning during use.
CooperSurgical is recalling lnflatoball Latex Rubber Pessaries because the secondary packaging incorrectly states the product is latex-free, despite being made of 100% latex.
Stryker is recalling 65 PROFESS Registration Kits shipped near or past their expiration dates. The kits are used for intranasal and sinus surgery.
Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 7.5 mg, because they failed impurity specifications. The recall covers 6,138 bottles distributed nationwide and in Puerto Rico.
Sun Pharmaceutical Industries is recalling specific lots of Olanzapine Tablets, 2.5 mg, because they failed impurity specifications.
Almore International Inc. is recalling Microfil Composite Instruments because packaging labels incorrectly display a sterile symbol, although the devices are not sterile.
Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 20 mg, because they failed impurity specifications. The recall covers 14,784 bottles distributed nationwide and in Puerto Rico.