State
73,806 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 178 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.
Which agencies issued them
These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
CareFusion is recalling Alaris System PC units because low battery alarms may fail to trigger before the battery discharges, stopping all infusion channels.
Merge Healthcare is recalling the Eye Station Import Utility software because system lockups may cause patient injury or delay diagnosis.
Merge Healthcare is recalling Merge Cardio software versions 9.0 through 9.0.8 because users can merge device files with confirmed reports, potentially adding unverified information.
Diamond Crystal Brands is recalling Chef's Companion Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.
Stanley Security Solutions is recalling 500 Arial Wireless Water-Resistant Call Pendants because they were incorrectly programmed, which may prevent alarms from sounding when the button is pressed.
Nidek Inc is recalling Final Fit Software versions 1.11 and 1.12 for the EC-5000 Excimer Laser System because treatment planning could be programmed with an unintended correction.
Diamond Crystal Brands is recalling specific lots of Natural Cocoa Powder because metal pieces were found missing from a sifter screen during sanitation.
Daimler Trucks North America is recalling one 2016 Thomas Built Buses Saf-T-Liner C2 school bus because the transmission grade brake may fail to deactivate, increasing crash risk in slippery conditions.
Juratoys is recalling four models of Bricolo by Janod push toy trolleys because they can tip backwards, posing an impact injury hazard to children.
Zydus Pharmaceuticals USA Inc. is recalling specific lots of Atenolol 50 mg tablets because a customer reported finding a paroxetine 20 mg tablet in a bottle.
Integra LifeSciences is voluntarily recalling Panta and Panta XI Nails because package seals may not maintain intended sterility.
Target is recalling about 19,000 magnetic tic tac toe games because the magnets can detach, posing choking and serious internal injury risks.
Manzana Products Co. is recalling Trader Joe's Organic Unsweetened Apple Sauce after customer complaints and inspections revealed small pieces of glass in the product.
Subaru is recalling 2017 Impreza vehicles because winter fuels may vaporize in the fuel line, causing engine stalling and increasing crash risk.
Manzana Products Co. is recalling Trader Joe's All Natural Unsweetened Apple Sauce after finding small pieces of glass in the product.
Purewick Corporation is recalling 176,863 units of the PureWick External Catheter for Women because the labeling failed to disclose the presence of dry natural rubber and incorrectly stated the product was latex-free.
Hitachi Medical Systems America Inc is recalling 210 Hitachi Oasis MRI Systems because image data transferred to workstations showed errors on the slice position reference image.
BioMerieux SA is recalling ETEST Fosfomycin FM1024 strips because internal testing does not support the current shelf-life claims.
BioMerieux SA is recalling ETEST Ceftazidime TZ256 strips because their shelf-life claims are not supported by internal testing.
Hitachi Medical Systems America Inc is recalling 25 Hitachi Echelon Oval MRI Systems because image data transferred to workstations showed errors on the slice position reference image.
Haag-Streit USA Inc is recalling EyeSuite i.8.2.1.0 software due to a risk that patient data may be stored under the wrong patient on the DICOM Server.
Merge Healthcare is recalling Merge Cardio software versions 9.0 through 10.1.2 because the study list fails to display STAT studies without a manual refresh.
Hitachi Medical Systems America Inc is recalling 68 Hitachi Echelon MRI Systems because image data transferred to workstations showed errors on the slice position reference image.
Siemens Medical Solutions is recalling 13 Syngo.plaza PACS systems nationwide due to software update issues. The recall is voluntary and has been terminated.
BioMerieux SA is recalling ETEST Ceftriaxone strips because their shelf-life claims are not supported by internal testing. The products were distributed worldwide.