State
73,495 recalls have nationwide distribution and so reach Iowa. 5,592 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,592 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 1,590 (28%) are Severe.
Which agencies issued them
These figures cover only the 5,592 recalls whose distribution notice names Iowa specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Dole Fresh Vegetables is recalling its 9.1oz Peppercorn Ranch Chopped Kit due to potential Listeria monocytogenes contamination. Affected products carry best-if-used-by dates of November 30, 2021 through January 8, 2022.
Dole Fresh Vegetables Inc is recalling approximately 2.3 million cases of Dole 8.3oz Spinach Miso Crunch Kit due to potential Listeria monocytogenes contamination. The product was distributed nationwide.
Dole Fresh Vegetables Inc is recalling Nature's Promise 5oz Organic Baby Kale Clamshell due to potential Listeria monocytogenes contamination. Affected products were distributed across numerous U.S. states.
Dole Fresh Vegetables is recalling American Blend vegetable products due to potential Listeria monocytogenes contamination. The recall affects over 2 million cases distributed across 35 states.
Dole Fresh Vegetables Inc is recalling approximately 2.3 million cases of Dole 10.2oz Chopped Bacon Caesar salad due to potential Listeria monocytogenes contamination. Affected products were distributed nationwide with Best if Used By dates between November 2021 and January 2022.
Dole Fresh Vegetables Inc is recalling multiple packaged romaine lettuce products due to potential Listeria monocytogenes contamination. The products were distributed across 37 states.
Dole Fresh Vegetables Inc is recalling Natures Promise 5oz Organic Baby Spring Mix Clamshell due to potential Listeria monocytogenes contamination. Affected products bear codes beginning with 'N' or 'Y' with Best if Used By dates from November 30, 2021 through January 8, 2022.
GE Healthcare is recalling 17,228 MR superconducting magnet systems because the cryogenic ventilation system may not meet required venting standards.
Microbiologics Inc is recalling KWIK-STIK QC Sets and Panels due to potential contamination with E. coli and Staphylococcus species. The affected product was distributed worldwide to laboratory testing facilities.
The Novalung Sensor Box may experience communication failures between its flow sensor and sensor box component, potentially disabling flow measurement and air bubble detection. The recall affects 115 units distributed across 16 US states.
Smith & Nephew is recalling the Acufex Access Advanced Positioning Kit because the products were shipped to a distribution center instead of the sterilizer and were not sterilized before distribution.
GE Healthcare Discovery MR450 MRI systems may have cryogen ventilation systems that do not meet required venting standards. The recall affects approximately 17,228 devices distributed in the U.S. and internationally.
GE Healthcare recalled 17,228 superconducting magnets, a component of SIGNA 1.5T MR systems, due to a cryogen ventilation system that may not meet venting requirements. Systems are distributed nationwide and internationally.
GE Healthcare is recalling approximately 17,228 SIGNA Creator and Explorer MRI systems due to potential defects in their cryogen ventilation systems that may not meet required venting standards.
GE Healthcare is recalling MRI superconducting magnets with cryogen ventilation system defects not meeting safety requirements. The recall affects 17,228 devices distributed across the US and internationally.
GE Healthcare is recalling 17,228 MR superconducting magnet components due to a cryogen ventilation system that may not meet required venting specifications.
Diagnostic control microorganisms manufactured by Microbiologics Inc are recalled for returning incorrect antibiotic susceptibility test results. These controls failed quality specifications and could cause inaccurate lab test results.
Avanos Medical is recalling the MIC Percutaneous Endoscopic Gastrostomy (PEG) Kit because the external retention bolster may be oversized relative to the tube. Approximately 2,652 units have been distributed in the US, Canada, and Chile.
GE Healthcare is recalling Discovery MR750w 3.0T MRI systems due to cryogen ventilation systems that may not meet FDA venting requirements. Approximately 17,228 devices were affected.
Amy's Kitchen is recalling its Vegan Organic Rice Mac & Cheese due to undeclared milk detected during testing. The product is labeled dairy-free, posing a risk to consumers with milk allergies.
The Universal Chuck instrument handle may loosen and release ball bearings onto the surgical field. If not recovered, these bearings could delay surgery and potentially cause infection or tissue damage.
Valco Baby is recalling Snap Duo Trend strollers because the front wheels can break off during use, causing the stroller to fall unexpectedly. Consumers should stop using the stroller immediately and contact Valco Baby for a free replacement wheel assembly.
DePuy Orthopaedics is recalling 3 units of ATTUNE REVISION DISTAL FEMORAL AUGMENT due to adhesive residue that could cause tissue irritation or infection if not detected before surgery.
GE Healthcare is recalling 17,228 MRI systems due to a potential defect in the cryogen ventilation system that may not meet venting requirements. This Class II recall affects systems distributed nationwide and internationally.
Daimler Trucks North America is recalling 2017-2021 Freightliner Cascadia trucks because brake lights may remain illuminated after braking. This increases crash risk by making drivers unaware of actual braking.