State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Respire Medical is recalling the Pink Series EF+ Oral Sleep Apnea Device because it may break during use.
Arrow International is recalling 416,055 PICC Catheter Trimmers because unsealed packaging may compromise product sterility. The recall covers units distributed in the US and 34 other countries.
Spartan Motors is recalling 1991-2018 Utilimaster Aeromaster and Walk-In Vans because front seat belts lack required retractors, increasing crash injury risk.
Arrow International is recalling Maximal Barrier Drapes because unsealed packaging may compromise product sterility. The recall affects 416,055 units distributed in the US and 34 other countries.
Arrow International is recalling SnapLock Catheter/Syringe Adapters because unsealed packaging may compromise sterility. The recall affects 416,055 units distributed in the US and 34 other countries.
Arrow International is recalling 416,055 two-lumen central venous catheterization kits because unsealed packaging may compromise product sterility.
Arrow International is recalling specific lots of ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kits because unsealed packaging may compromise sterility.
Arrow International Inc is recalling 416,055 ARROW PICC Sets because unsealed packaging may compromise product sterility.
Arrow International is recalling TheraCath Epidural Catheters because unsealed packaging may compromise sterility. The recall covers 416,055 units distributed in the US and 33 other countries.
Arrow International Inc is recalling 10 cc Luer-Slip Loss of Resistance Syringes because unsealed packaging may compromise product sterility.
Arrow International Inc is recalling 416,055 Spring-Wire Guide Introducer Catheter Assemblies because the packaging may be unsealed, potentially compromising product sterility.
Arrow International is recalling 416,055 Echogenic Introducer Needles because unsealed packaging may compromise product sterility.
Arrow International Inc. is recalling Arrow-Flex Percutaneous Sheath Introducer Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 central venous catheterization kits because unsealed packaging may compromise product sterility.
Arrow International is recalling 416,055 ARROWgard Blue PLUS Triple-Lumen CVC Kits because unsealed packaging may compromise sterility.
Maquet SAS is recalling 187 VOLISTA StandOP surgical lights because the keypads may fail. The units were distributed worldwide from October 2012 to June 2017.
Arrow International is recalling Extension Line Slide Clamps because unsealed packaging may compromise product sterility. The recall affects 416,055 units distributed in the US and 34 other countries.
Arrow International Inc. is recalling Arterial Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling Radial Artery Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International Inc. is recalling 416,055 ARROW JACC IV catheters because unsealed packaging may have compromised product sterility.
Arrow International is recalling 416,055 Pressure Injectable Multi-Lumen Central Venous Catheterization Kits because unsealed packaging may compromise product sterility.
Arrow International is recalling specific lots of Percutaneous Sheath Introducer Kits because unsealed packaging may compromise product sterility.
NordicNeuroLab AS is recalling 16 licenses of nordicTumorEx 1.0 software because a DICOM header error may cause incorrect image orientation labeling.
GE Lighting is recalling LED tube lamps sold at Lowe's because the pins can become energized during installation, posing electric shock and electrocution hazards.
Medline is recalling sterile needle counters because packaging seal creep may compromise sterility. The product is used to count surgical sharps.