State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pinook-Usa is recalling 28,994 Pinook Micro Massagers because the company failed to submit a premarket submission and gain FDA approval for the device.
Smiths Medical is recalling Portex Spinal Anaesthesia Trays because some included glass ampules contain visual particulate matter.
Beckman Coulter is recalling ISE REF Valves for AU480, AU680, and AU5800 analyzers due to premature valve failure that may affect test accuracy.
Source Naturals is recalling GABA dietary supplements because a metal fragment was found in a tablet during inspection.
Smiths Medical ASD, Inc. is recalling 140 Portex Spinal Trays because visual particulate was found in the included Lidocaine and Dextrose ampules.
Beckman Coulter is recalling ISE REF Valves for AU series chemistry analyzers because premature valve failure may affect test accuracy.
Insulet Corporation is recalling 5,050 OmniPod Insulin Management Product Demonstration Kits because the included alcohol prep pads are not properly labeled.
Smiths Medical is recalling Portex Spinal Trays because visual particulate was found in the lidocaine and dextrose ampules.
Pinook-Usa is recalling 28,994 Pinook Mini Massagers because the company failed to submit a premarket submission and gain approval for the medical device.
Smith & Nephew is recalling four units of Genesis II tibial base implants due to packaging errors where size 5 left and size 6 right components were swapped.
Insight Instruments is recalling MLS Torpedo Mini-Light Ophthalmic illuminators because the product was registered as a Class I device but is actually a Class II device requiring FDA clearance.
Helix Medical LLC is recalling 47 units of the Blom-Singer Adjustable Tracheostoma Valve II because the essential body component is missing from the packaging, rendering the device unusable.
Intuitive Surgical is recalling da Vinci Vision System Cart components due to a coating incompatibility that triggers erroneous maintenance alerts.
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Intact PTH Calibrators because some kits were packaged with only the high calibrator.
L.L. Bean is recalling about 800 girl's pajama sets because they fail to meet federal flammability standards, posing a risk of burn injuries.
Babycottons is recalling about 1,100 children's nightgowns because they fail to meet federal flammability standards, posing a risk of burn injuries.
Wood Castle Furniture is recalling Riley Duo bunk beds because guardrail openings may be too wide, posing an entrapment risk to children.
BMW is recalling specific 2006-2007 models because the front passenger seat sensor may crack, potentially deactivating the air bag in a crash.
Indiana Mills and Manufacturing Inc. is recalling seat belt assemblies manufactured between August and October 2013 that may fail to release properly, potentially hindering vehicle egress during emergencies.
PROLine is recalling 2010-2013 travel trailers because auxiliary batteries lack proper overcurrent protection, creating a fire risk if wiring is damaged.
Terex Advance is recalling 2013 concrete trucks because a front axle u-bolt can fracture, potentially causing the axle to separate and leading to a crash.
Toyota is recalling 2013-2014 Tacoma vehicles because engine valve springs may break, potentially causing the engine to stall while driving and increasing crash risk.
Forest River is recalling 2012-2013 Rockwood, Windjammer, Vlite, and Flagstaff travel trailers because tires may contact the floor, risking blowouts and loss of control.
Jayco is recalling 2011 Jay Series pop-up camping trailers because a roof lifter failure could cause the roof to collapse, increasing injury risk.
Starcraft RV is recalling 2013 RT and Comet pop-up camping trailers because a roof lifter failure could cause the roof to collapse, increasing injury risk.