State
73,190 recalls have nationwide distribution and so reach Iowa. 5,590 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,590 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 1,320 (24%) are Severe.
Which agencies issued them
These figures cover only the 5,590 recalls whose distribution notice names Iowa specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Racine Danish Kringles Raspberry Kringle (14 oz., lot 23299) is being recalled due to undeclared tree nuts (pecans). Consumers with nut allergies should not consume this product.
Zimmer Biomet Spine Inc. is recalling Vitality Polyaxial Screws (7.5mm x 50mm) due to incorrect laser marking showing 7.5 x 40. Incorrect screw size could cause perforation and vascular damage during spinal surgery.
Medtronic is recalling Protege GPS Self-Expanding Peripheral Stent Systems due to seal defects in product packaging that could compromise sterility. Affected lot B644679 had national distribution.
Merit Medical Systems is recalling specific lots of microcatheter and infusion system devices because their sterility cannot be guaranteed. The devices were distributed worldwide including multiple US states and international locations.
Natus Medical Incorporated is recalling 2,686 units of External Drainage System Collection Bags due to incomplete bioburden testing that prevents sterility assurance. Healthcare facilities and patients should contact the manufacturer or their healthcare provider for guidance.
Azurity Pharmaceuticals recalls Eprontia (topiramate) oral solution nationwide because routine stability testing found an out-of-specification impurity. The chemical defect raised concerns about the drug's purity and patient safety.
Abiomed has disabled four features in the Impella Connect software portal because the FDA has not evaluated them for safety and effectiveness.
Encore Medical is recalling 17 Reverse Shoulder System e+ surgical implants (Lot 381P1167) due to mislabeling. Affected units were distributed nationwide to multiple states.
Keystone Industries is recalling 336 units of KeySplint Hard Clear due to incorrect Instructions for Use packaged with the product. Affected units received KeySplint Soft instructions instead.
Encore Medical has voluntarily recalled a patella implant component (REF 130-03-738) due to mislabeling. The recall involves 2 units distributed nationwide.
PL Custom is recalling 2020-2024 Type 1 and Type 3 ambulances because a firmware defect may cause electrical circuits to overheat and catch fire.
Alexis Fire Equipment is recalling 56 fire trucks from 2022-2023 because a firmware defect may prevent electrical circuits from shutting off, increasing fire risk.
E-One is recalling 408 fire trucks because a wiring defect may cause electrical circuits to overheat and start a fire.
Marion Body Works is recalling 2024 Spartan Fire MetroStar vehicles because a defective inversion valve may delay parking brake engagement, increasing the risk of unintentional vehicle movement.
Forest River is recalling Coachmen Galleria motorhomes (2020–2024) because battery boost wiring may become damaged, causing an electrical short circuit that results in loss of power steering, increasing crash risk.
Forest River is recalling 2020 Cherokee travel trailers because the draw bar locking mechanism may break, causing the trailer front to contact the road and increasing crash risk.
Salm Partners, LLC is recalling ready-to-eat turkey kielbasa products due to possible contamination with bone fragments.
Mickey Truck Bodies is recalling 37 commercial trucks from 2020-2023 because exposed wiring on the refrigeration unit may cause electrical arcing and increase fire risk.
Terex Advance is recalling 2023-2024 concrete mixer trucks because bolts may loosen, causing the drum to separate from the vehicle.
Braun Northwest is recalling 2020-2021 Northstar ambulances because a firmware defect may cause electrical circuits to overheat and increase the risk of fire.
Ride Aventon is recalling about 2,300 Class 2 Sinch.2 folding e-bicycles because they can accelerate unexpectedly, causing loss of control and crash hazards. The firm has received six reports of unexpected acceleration but no injuries.
Bell Sports is recalling about 2,360 Bell Slope Adult Helmets because the strap anchor can dislodge during impact, violating safety standards and risking head injury in a crash.
UBBCARE play yard mattresses violate federal safety standards for crib mattresses and pose a suffocation hazard to infants. The mattresses are missing required warnings and labels and fail thickness tests. No injuries have been reported.
Homedics is recalling about 46,000 Therapist Select Percussion Personal Massagers (model HHP-715) because they can overheat while charging, creating fire and burn risks. The company has received 17 overheating reports, including one burn injury.
H.H. Brown Shoe Company is recalling about 2,360 Redeemer DH 5379 work boots sold from February 2023 through October 2023 because the sole is not puncture-resistant, posing an injury hazard. No injuries have been reported.