State
73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Arrow International is recalling 8 units of the AutoFuser Disposable Pain Control Pump due to possible cracks on the fill port connector that may cause leaks.
Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that may cause leaks and reduced drug delivery.
Philips is recalling 11,226 Intera 0.5T MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling 11,226 Ingenia Ambition X MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Cardinal Health is recalling Curity All Purpose Sponges because they were not sterilized. The affected units were distributed in the US, Canada, and Colombia.
Philips is recalling SmartPath to dStream MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling 11,226 Ingenia 3.0T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Multiva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Intera Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Enterprise 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Achieva 3.0T MRI systems because ceiling speakers may fall due to magnetic attraction.
Philips is recalling Multiva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling 11,226 Achieva 3.0T X MRI systems because ceiling speakers may fall due to the magnetic field.
Philips is recalling Intera 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Philips is recalling Intera Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Zimmer Biomet Spine Inc. is recalling Vitality Shear-off Set Screws because they do not thread properly with mating components due to a manufacturing issue.
Philips is recalling Intera Achieva 1.5T MRI systems because ceiling speakers may be pulled by the magnetic field and fall.
Arrow International is recalling specific AutoFuser pumps due to possible cracks in the fill port connector that could cause leaks and reduced drug delivery.
Philips is recalling 11,226 Ingenia 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Porsche is recalling 2018 Panamera models because incorrect soldering on a control unit may cause intermittent system failures and impaired driveability.
Philips is recalling 11,226 Achieva 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Arrow International Inc is recalling specific Arrow AutoFuser Disposable Pain Control Pumps due to possible cracks on the fill port connector that may cause leaks and reduced drug delivery.
Philips is recalling Ingenia 1.5T MRI systems because ceiling speakers may fall and be pulled by the magnetic field.
Fenton Mobility is recalling 2015-2017 Ford Transit vans with wheelchair lifts that may fail to comply with safety standards, posing a tip-over risk.