State
72,919 recalls have nationwide distribution and so reach Iowa. 5,581 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,581 recalls naming Iowa we have scored against our rubric, 909 (16%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,317 (24%) are Severe.
Which agencies issued them
These figures cover only the 5,581 recalls whose distribution notice names Iowa specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
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.
USDA FSIS issued a public health alert for meat and poultry products containing FDA-regulated dairy ingredients that may be contaminated with Salmonella. No illnesses have been reported to date.
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.
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.
Travel Size Afrin Original Nasal Spray 6 mL bottles are recalled because the packaging does not meet Poison Prevention Packaging Act requirements for imidazolines.
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.
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.
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.
Medline Industries, LP is recalling Medline Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects approximately 270,311 units distributed worldwide.
Dorman is recalling specific transmission gearshift cables where the bushing may detach, preventing the vehicle from shifting into Park and increasing the risk of a crash.
B. Braun Medical Inc. is recalling Dextrose Injection USP 70% in 2000 mL bags nationwide due to lack of assurance of sterility and potential leakage from the diaphragm port after foil removal.
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.
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.
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.
Medline Industries is recalling select Convenience Kits containing 10mL polycarbonate colored syringes (Eye Pack and Heart Cath Pack) due to unapproved design changes made outside of FDA 510(k) clearance.
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 approximately 270,311 units distributed in the US and internationally.
B. Braun Medical Inc. is recalling Sterile Water for Injection USP 3000 mL bags (24,928 units) distributed nationwide due to lack of assurance of sterility and potential leakage from the diaphragm port.
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 Convenience Kits containing 10mL Polycarbonate Colored Syringes due to unapproved design changes made outside of FDA 510(k) clearance. The recall affects multiple product SKUs distributed nationwide and internationally.
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 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.
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.
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 Convenience Kits containing 10mL polycarbonate colored syringes because the products were modified in ways not approved by the FDA. The kits were distributed nationwide and internationally.