State
73,100 recalls have nationwide distribution and so reach Iowa. 5,588 additional recalls listed Iowa specifically in their distribution scope.
Of the 5,588 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 1,319 (24%) are Severe.
Which agencies issued them
These figures cover only the 5,588 recalls whose distribution notice names Iowa specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
A software issue in the BD PYXIS MDBNK medication dispensing cabinet may cause restock labels to print with incorrect bin locations, potentially affecting medication storage accuracy.
Olympus is recalling Everest Bipolar Cutting Forceps due to fractures and breakages in packaging trays and Tyvek covers that may compromise sterility. The recall affects 4,364 units distributed worldwide.
The BD PYXIS MEDBANK MINI automated dispensing cabinet software may print incorrect bin locations on restock labels, potentially causing medications to be placed in wrong locations.
American Contract Systems is recalling Hand Pack convenience kits that may not be sterile due to insufficient aeration time during sterilization. Affected devices distributed in CA, KS, ME, MN, MO, NE, and SD may pose a safety risk.
CareFusion's BD PYXIS medication dispensing cabinet with software version 3.9.1.9 may print incorrect bin labels during restocking, potentially leading to wrong medication dispensing. Eleven units distributed nationwide are affected.
American Contract Systems is recalling 224 Biopsy Drape Pack convenience kits due to insufficient aeration time during sterilization, which may have compromised the sterility of affected units. Lot 981241 distributed in CA, KS, ME, MN, MO, NE, and SD is affected.
American Contract Systems is recalling Special Procedure Pack convenience kits due to insufficient aeration time during sterilization, which may have compromised sterility. Distributed in California, Kansas, Maine, Minnesota, Missouri, Nebraska, and South Dakota.
The support arm on Siemens Multitom Rax X-ray systems may unintentionally lower, creating a fall risk to people positioned beneath the ceiling-mounted display during system positioning.
BioFire Diagnostics is recalling gastrointestinal diagnostic test kits due to false positive Vibrio results when used with certain transport mediums.
Certain 2019-2025 Holiday Rambler Admiral and other RVs have exterior patio outlets lacking GFCI protection when powered by generator or shore cord, increasing electrical shock risk. Dealers will install GFCI devices free of charge.
The Soltive Premium SuperPulsed Laser System may experience difficulties pairing its wireless footswitch, potentially delaying surgical procedures. The recall affects units distributed worldwide.
Urban River Spirits is recalling Ruby-Red Grapefruit Mixer due to potential under-processing of the non-alcoholic beverage made in an unlicensed facility. No illnesses have been reported.
Urban River Spirits is recalling Peppered Peach Bliss, a non-alcoholic cocktail mixer, due to potential under-processing risks. The product was manufactured in an unlicensed and uninspected facility.
Olympus Corporation is recalling the Soltive Pro SuperPulsed Laser System due to difficulties pairing its wireless footswitch, which could delay surgical procedures. The recall affects 253 units worldwide.
Urban River Spirits is recalling Raspberry and Peach Melody non-alcoholic cocktail mixer due to concerns over potential under-processing. The product was manufactured in an unlicensed and uninspected facility.
Urban River Spirits is recalling 3,876 bottles of Spicy Cool-aid: Watermelon & Jalapeno due to potential under-processing. The product was manufactured in an unlicensed and uninspected facility.
Urban River Spirits' Spicy Orange and Mango Fusion non-alcoholic cocktail mixer is recalled due to production in an unlicensed, uninspected facility with potential under-processing. Approximately 3,876 bottles were distributed across 11 states.
Urban River Spirits recalls 3876 bottles of Maple Infused Simple Syrup distributed across multiple states. The product was manufactured in an unlicensed, uninspected facility and may be under-processed.
Urban River Spirits Life s a Peach Spritzer is recalled because it was manufactured in an unlicensed, uninspected facility with potential under-processing. No illnesses have been reported.
Urban River Spirits is recalling its Lemon Drop Mixer due to being manufactured in an unlicensed, uninspected facility with potential under-processing concerns affecting product safety. The product was distributed across multiple states.
Urban River Spirits voluntarily recalls Velvet Cocoa and Caramel cocktail mixer due to potential under-processing from manufacture in an unlicensed, uninspected facility. Product distributed across 11 states.
Urban River Spirits is recalling Pear-Tini Mixer because it was made in an unlicensed and uninspected facility. The product may not have been properly processed.
Cafe Caramel Delight, a non-alcoholic cocktail mixer, is being recalled because it was produced in an unlicensed, uninspected facility with potential under-processing concerns.
Urban River Spirits is recalling Lush Lavender & Wildberry Spritz non-alcoholic mixer due to potential under-processing. The product was manufactured in an unlicensed and uninspected facility.
Urban River Spirits is recalling Summer Sunset Strawberry and Peach non-alcoholic cocktail mixer from multiple states because it was manufactured in an unlicensed and uninspected facility, creating potential under-processing concerns.