State
72,984 recalls have nationwide distribution and so reach Iowa. 5,585 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,585 recalls naming Iowa we have scored against our rubric, 910 (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 5,585 recalls whose distribution notice names Iowa specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
General Motors is recalling 2025 Chevrolet Express and GMC Savana vehicles because the front passenger seat head restraint may be improperly welded, increasing injury risk in a crash.
About 3,400 Xylolin peg doll toy sets sold on Amazon.com are being recalled because the spherical ends of the peg dolls can block a child's airway, posing a choking risk. Consumers should take the product away from children immediately and dispose of it.
Delta-branded Gas Ball Valves pose fire and burn hazards because small amounts of gas can leak from the valve when it is in the open position. About 3,700 units were sold in the United States.
Yamaha Corporation of America is recalling about 37,400 PA-300C AC power adaptors that can overheat and ignite. The company has received four reports of adaptors burning or smoking, though no injuries have been reported.
Volvo is recalling certain 2021-2025 vehicles because the rearview camera image may not display when the vehicle is placed in reverse. 413,151 units are affected.
Sanven Technology recalls approximately 800 Vevor stainless steel cable railing kits sold online from May 2021 through September 2024 because the bottom hole on the cable support posts poses an entrapment hazard to children.
Chrysler is recalling certain 2022-2025 Pacifica and Voyager vehicles because improperly sealed seams may leave the side curtain airbags with insufficient pressure retention.
DEMDACO is recalling approximately 3,000 Maril Brand 8-ounce scented candles because the glass container can crack or break while burning, posing laceration and fire hazards. Three incidents of glass breaking have been reported, with no injuries or property damage so far.
Legend Brands is recalling approximately 500 Bliss hair dryers due to lack of immersion protection, which can cause death or serious injury from electrocution if the dryers fall into water while plugged in. No injuries have been reported.
Thor Motor Coach is recalling 2025-2026 Outlaw motorhomes because step bracket bolts may loosen, allowing steps to detach and increase injury risk.
Deuter USA is recalling Kid Comfort, Kid Comfort Pro, and Kid Comfort Active Child Carriers because hinges on the foldable rear kickstand support leg can crack or break, creating a fall hazard. No injuries have been reported.
GE Healthcare is recalling certain Carestation 620/650/650c and 750/750c Anesthesia Delivery Systems because they may not provide effective ventilation in Volume Control Ventilation (VCV) mode. The issue does not affect Pressure Control Ventilation (PCV), PCV-VG, or manual ventilation modes.
Certain GE Healthcare CARESTATION 620, 650, 650c, 750, and 750c anesthesia delivery systems may not provide effective ventilation in Volume Control Ventilation (VCV) mode. Effective ventilation is available using other ventilation modes or manual ventilation.
Certain GE Healthcare Carestation anesthesia delivery systems may fail to provide effective ventilation in Volume Control Ventilation (VCV) mode. Affected systems can still be used safely in Pressure Control Ventilation or Manual ventilation modes.
GE Healthcare is recalling certain Carestation 620 SE anesthesia systems (27 units) because they may not provide effective ventilation in Volume Control Ventilation mode. Alternative ventilation modes remain functional.
Medtronic Enhanced Verify Evaluation Handsets (CFN HH90130FA) may fail to communicate with neurostimulators due to faster processing speed, causing therapy to stop and patients to experience return of underlying symptoms.
Certain GE Healthcare CARESTATION 750 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Affected systems can deliver ventilation through alternative modes or manual ventilation.
Certain GE Healthcare Carestation 650 A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Alternative ventilation modes or manual ventilation can be used.
Waldemar Link GmbH & Co. KG is recalling Tibial Augment devices distributed nationwide because preassembled Femoral Augment screws were delivered missing their threads.
Waldemar Link is recalling Posterior Femoral Augments used in knee surgery because some units were delivered with a preassembled screw missing its thread, which could compromise surgical fixation.
GE Healthcare CARESTATION 750c A1 anesthesia systems may not provide effective ventilation in Volume Control Ventilation mode. Affected units can achieve ventilation through alternative modes or manual operation.
GE Healthcare CARESTATION 620 A1 anesthesia systems may fail to provide effective ventilation in Volume Control Ventilation mode. Effective ventilation is available in Pressure Control or Manual ventilation modes.
Waldemar Link GmbH & Co. KG is recalling Distal Femoral Augment devices because the preassembled femoral augment screw was missing its thread. The defect may affect proper device function.
GE Healthcare CARESTATION anesthesia delivery systems may fail to provide effective ventilation in Volume Control Ventilation mode. Affected units can deliver ventilation through Pressure Control Ventilation modes or manual ventilation.
Certain GE Healthcare CARESTATION 750 A2 anesthesia systems may not provide effective ventilation in Volume Control Ventilation mode. Users should switch to Pressure Control Ventilation or Manual ventilation modes.