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.
Load Trail is recalling 2018-2019 dump trailers because bolts on the hydraulic cylinder can break under heavy loads, causing the dump box to lower rapidly.
Audi is recalling 2018-2019 Q5 and SQ5 vehicles because a short brake master cylinder casting could cause sudden brake loss, increasing crash risk.
Ford is recalling 2015-2019 F-150 and 2017-2019 Super Duty trucks because a damaged block heater cable could cause a fire.
Nova Bus is recalling 2011-2019 LFS city buses because an engine door fan electrical connector may overheat and cause a fire.
J&J Snack Foods Handhelds Corp. is recalling Bremer hot stuffed sandwiches due to possible semi-transparent plastic contamination. No illnesses have been reported.
PACCAR is recalling 2018-2020 Kenworth T680 and T880 trucks because a parking brake signal delay in cold weather may cause unexpected vehicle movement.
BMW is recalling 2006 3, 5, and Z4 series vehicles because a heater in the PCV valve may short circuit, increasing the risk of a fire.
Blount Fine Foods is recalling frozen chicken soup products due to misbranding and an undeclared milk allergen. No adverse reactions have been reported.
Vivitar is recalling hot/cold massage balls sold at Target because they can leak or rupture during microwaving, posing a burn hazard.
Mazda is recalling 2016-2018 Mazda3 vehicles because a defective wiper relay may cause the wipers to stop working, reducing visibility and increasing crash risk.
Ata International Inc is recalling Blue Fusion Capsules because FDA analysis found undeclared prescription ingredients, including Sildenafil and Tadalafil.
Maquet Cardiovascular is recalling 10 units of the Cardiohelp Emergency Drive because the gearwheel may have been incorrectly reassembled, leading to inadequate operation.
Philips is recalling UroDiagnost MRF units because a missing locking plate may cause unexpected stand or table tilt movement that users cannot stop.
Philips North America is recalling 1,696 OmniDiagnost Classic X-ray systems because a missing locking plate may cause unexpected stand or table movement that users cannot stop.
Weis Fire & Safety is recalling one 2018 Ford F-550 emergency vehicle because its brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.
Beaver Visitec is recalling specific lots of Soft Tip Cannulas because a missing protective sheath may cause the silicone tip to break or detach during eye procedures.
Medical Action Industries is recalling specific lots of laparotomy sponges due to a potential lack of sterility assurance. The affected products were distributed nationwide and to Canada and Saudi Arabia.
LW Scientific is recalling ZIP IQ Combo Centrifuges because the hematocrit rotor may break and eject through the housing, posing a safety hazard.
Becton Dickinson is recalling BD Synapsys version 2.1 because it allowed test orders to be associated with incorrect culture records.
Hometown Food Company is recalling Pillsbury Unbleached All Purpose Flour due to potential Salmonella contamination. The product was distributed nationwide.
Accelerate Diagnostics is recalling 81 Accelerate Pheno systems because rare bacterial isolates may generate incorrect meropenem susceptibility results. A software update suppresses these specific results to mitigate risk.
GE Healthcare is recalling 288 integrated ECG cables that can short circuit during defibrillation, potentially diverting 25% of the energy away from the patient.
Philips North America is recalling 40 lithium-ion rechargeable batteries for the MX40 Wearable Monitor due to a manufacturing defect that may affect monitor operation.
Mobility Specialists is recalling 2014-2017 Ford E-150 and Transit vans with wheelchair lifts that may fail, posing a tipping risk to users.
LW Scientific is recalling 142 ZIP IQ PCV Centrifuges because the plastic rotor may break and be ejected, posing a safety hazard to technicians.