State
72,969 recalls have nationwide distribution and so reach Indiana. 9,556 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,556 recalls naming Indiana we have scored against our rubric, 1,903 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,136 (22%) are Severe.
Which agencies issued them
These figures cover only the 9,556 recalls whose distribution notice names Indiana specifically. The 72,969 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Forest River is recalling 2026 Westbrook and Tracer recreational trailers because a liquid propane gas hose may rub against the furnace, causing a fuel leak that increases fire risk.
Ozark Trail 64 oz Stainless Steel Insulated Water Bottles are being recalled because the lid can forcefully eject on opening. Three injuries are reported, including two cases of permanent vision loss.
Mitsubishi Fuso is recalling 2024-2025 Rizon trucks because an oversized spacer in the electric parking brake may cause overheating and fire.
AUGNORYE padded cushioned crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct an infant's breathing. About 356 units are affected.
Momentum Vida E+ e-bikes are being recalled because the fork steerer tube can crack, break or separate during use, posing a fall hazard. About 6,200 units are affected.
SPPTTY kids 14- and 18-inch bicycles are being recalled because multiple components contain lead exceeding the federal lead content ban. About 200 units are affected.
Creekliybear "Pack and Play" aftermarket play yard mattresses are being recalled because they exceed thickness requirements and may not fit certain play yards. About 21,500 units affected.
Dearlomum retractable mesh safety gates are being recalled because a child's torso can fit through the opening between the gate and the floor. About 2,200 units are affected.
WLIVE Fabric 15-Drawer Dressers are being recalled because they are unstable if not anchored to the wall and violate the federal standard under the STURDY Act. About 6,600 units affected.
Unbranded braided crib bumpers are being recalled because they violate the federal crib bumper ban and can obstruct breathing. About 260 units are affected.
Zicam Nasal AllClear swabs are being recalled because of fungal contamination of the nasal swabs. All lots are affected, covering 13,632 cartons.
Tailstorm Health INC is recalling Lidocaine HCL Sterile Injection (20 mg/mL) due to FDA inspection findings of concerns with the sterile manufacturing process. The recalled product is distributed nationwide.
Orajel Baby Cooling Swabs for Teething are being recalled because of fungal contamination of the infant oral swabs. All lots are affected, covering 695,880 cartons.
JFE Franchising Inc. is recalling Yaki Noodle Bowls and Ebi Vermicelli Bowls due to potential Salmonella contamination in cucumbers used in the products.
A range of packaged salads is being recalled because the cucumbers used in them have the potential to be contaminated with Salmonella. Affected product carries a sell by date of 5/20/2025.
Zicam Cold Remedy Medicated Nasal Swabs are being recalled because of fungal contamination of the swabs. All lots are affected, covering 3,374,918 cartons.
Servo-u MR Ventilator System (Model 6888800) may measure patient circuit compliance inaccurately due to incorrect pre-use leakage testing and incorrect active humidifier use.
Buffered Penicillin G Potassium for Injection is being recalled because some vials of cefazolin for injection were incorrectly labeled as penicillin G potassium 20 million units.
Philips Ultrasound, Inc is recalling 5,230 Philips 3D9-3v Transducer devices because they were refurbished beyond their useful life, posing a risk of device failure during medical use.
Brown shell eggs sold under numerous retail brands are being recalled because of potential contamination with Salmonella. The action covers 20,400,000 eggs, or 1,700,000 dozen.
The Philips Respironics BiPAP V30 Auto Ventilator is being recalled because the device does not indicate for use in patients with respiratory failure. 5,958 units affected.
Sandoz Cefazolin for Injection 1 gram is being recalled after cartons were found to contain vials labeled as penicillin G potassium. 208,300 vials are affected.
Philips Respironics is recalling BiPAP A30 and BiPAP Hybrid A30 ventilators. The devices do not have an indication for use in patients with respiratory failure.
The Servo-n Ventilator System is being recalled because patient circuit compliance may be measured inaccurately during the patient circuit test. 7,688 units affected.
JFE Franchising Inc. is recalling multiple fruit and vegetable tray products because cucumbers may be contaminated with Salmonella. The affected products were distributed in seven states with a sell-by date of May 20, 2025.