State
72,919 recalls have nationwide distribution and so reach Indiana. 9,555 additional recalls listed Indiana specifically in their distribution scope.
Of the 9,555 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 9,555 recalls whose distribution notice names Indiana specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
DGIVOVO US electric pressure washers are recalled because they lack an integral ground-fault circuit interrupter, posing shock and electrocution hazards. 50 units are affected.
Qumeney Bicycle Light Sets are recalled because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. About 2,800 units are affected.
StrikeLock hoistway door locking devices for residential elevators are recalled because they can allow the elevator cab to move with a landing door open, posing a fall hazard.
Earthtec 7 3/8 inch pool drain covers are recalled because they violate the entrapment protection standards of the Virginia Graeme Baker Pool and Spa Safety Act.
Malker Bicycle Light Sets are recalled because they contain button cell batteries that can be accessed easily by children, posing an ingestion hazard. About 7,000 units are affected.
UHOMEPRO 5-Drawer Dressers are recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children. About 5,190 units are affected.
Hepo adult portable bed rails are recalled because users can become entrapped within the rail or between the rail and the mattress. About 2,200 units are affected.
1-K Kerosene Heater Fuel portable containers are recalled because they lack the flame mitigation devices required under the Portable Fuel Container Safety Act. About 30,155 units are affected.
Travel Size Afrin Original Nasal Spray 6 mL bottles are recalled because the packaging does not meet Poison Prevention Packaging Act requirements for imidazolines.
Segmart 4-Drawer Dressers are recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children. About 16,440 units are affected.
Build-A-Bear Workshop Heartwarming Hugs Bears are recalled because the zipper slider on the side pouch can detach, posing a choking hazard to children. About 36,000 units are affected.
Acer AES015 folding electric scooters are recalled because a loose screw can cause the front tube to fold down unexpectedly, posing a fall hazard. About 510 US units are affected.
LSL Healthcare is recalling its Infant Central Line Dressing Change Kit (Model 2925H) distributed nationwide because it contains Webcol Large Alcohol Prep Pads that were recalled for non-sterility.
Medline Industries is recalling Medline Convenience Kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA 510(k) clearance. The kits were distributed nationwide in the US and to Canada, Panama, and Barbados.
Harrow Eye LLC is recalling FRESHKOTE Lubricant Eyedrops because the manufacturer cannot guarantee the product remains sterile. Affected lots are 1X68 and 1X69, with an expiration date of 05/31/2027.
Medline Industries is recalling 12 types of angiography and catheter kits because their 510(k) regulatory clearances have been rescinded. The kits were distributed nationwide.
LSL Healthcare is recalling IV Start Kits containing Webcol Large Alcohol Prep Pads due to non-sterility concerns. The affected kits were distributed nationwide in Maryland, Illinois, and Minnesota.
Medline Industries has recalled Control Syringes (Model DNSC89369 and DYNJSYR10C), Guidewires, and High-Pressure Tubing after their FDA 510(k) regulatory clearances were rescinded. The devices were distributed nationwide.
Medline Industries is recalling certain Labor Pack kits (Model DYNJ44813D) nationwide because their 510(k) regulatory clearances for Control Syringes, Guidewires, and High-Pressure Tubing have been rescinded.
Medline Industries has recalled its PICC Tray (Model DYNJ41648A) because the 510(k) regulatory clearances for certain Control Syringes, Guidewires, and/or High-Pressure Tubing have been rescinded by FDA.
B. Braun Medical Inc. is recalling sodium chloride for irrigation solution (3000 mL bags) due to lack of assurance of sterility and potential leakage from the diaphragm port. Affected lots distributed nationwide have expiration dates through May 31, 2028.
Medline Industries is recalling multiple Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects products distributed worldwide including the US, Canada, Panama, and Barbados.
Medline Industries is recalling 41 different surgical kit models nationwide because regulatory clearances for certain control syringes, guidewires, and high-pressure tubing have been rescinded. Affected facilities should stop use and contact Medline.
Kirkland Signature Traditional Madeleines are being recalled because packages were filled with heart madeleines containing undeclared hazelnut and soy lecithin. 92 units are affected.
Angiodynamics, Inc. is recalling Soft-Vu Angiographic Catheter (Straight Art, Non-Braided) units due to a manufacturing defect that may prevent guidewires from passing through the catheter hub's inner diameter.