State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Pharmatech LLC is recalling Senna Syrup due to a precautionary measure regarding potential contamination with B. cepacia bacteria.
Pharmatech LLC is recalling 1,008 bottles of Sennazon (sennosides) Syrup nationwide due to a potential risk of contamination with B. cepacia bacteria.
Pharmatech LLC is recalling Diocto Syrup (docusate sodium) nationwide due to a potential risk of contamination with B. cepacia bacteria.
Medtronic is recalling CareLink iPro Version 1.10 software due to a time stamp error. The recall affects 33 units distributed nationwide.
Pharmatech LLC is recalling Ninjacof cough syrup due to a potential risk of contamination with B. cepacia bacteria.
Pharmatech LLC is recalling Ninjacof-A liquid due to a potential risk of contamination with B. cepacia bacteria. This is a precautionary measure.
EKOS Corporation is recalling 455 EKOS carts because missing washers may cause wheels to wear or dislodge, leading to equipment failure.
Siemens is recalling ADVIA Centaur Calibrator U kits due to failure of analytical sensitivity and drift from internal standardization.
Prismatik Dentalcraft is recalling 150 units of BruxZir Shaded dental restorations because the manufacturer failed to properly identify quarantined lots as such.
Mckesson Packaging Services is recalling 181 cartons of Lansoprazole capsules due to a label mix-up where the outer packaging was mislabeled.
Ethicon, Inc. is recalling Mersilene Tape products because certain product codes were supplied with an incorrect Instructions for Use (IFU) insert.
Unichem Pharmaceuticals is recalling 368 bottles of Lamotrigine 150 mg tablets because they have the wrong imprint. The FDA classifies this as Class III.
Pfizer is recalling 1,316 bottles of Premarin 1.25 mg tablets because they were labeled with an incorrect expiration date of 11/17 instead of 09/17.
Daimler Trucks is recalling 2017 Freightliner Custom Chassis S2 vehicles because the brake transmission shift interlock may fail, allowing the vehicle to move unintentionally.
FULLBEAUTY Brands is recalling approximately 31,500 children's nightgowns because they fail to meet federal flammability standards, posing a risk of burn injuries.
Interlogix is recalling about 67,000 wireless personal panic devices because they may fail to operate during an emergency. Consumers should contact their security installer for a free inspection and replacement.
Sargent Art is recalling 13 types of tempera and finger paints due to potential harmful bacteria. Consumers should stop using the products and contact the company for a refund.
REV is recalling 2010-2016 Road Rescue and other emergency vehicles because touchscreen software may cause accessories to turn on or off unexpectedly, increasing crash risk.
Office Depot is recalling Winsley Mid-Back Chairs because they can tip over when users lean back, posing a fall hazard. No injuries have been reported.
Kia is recalling 12,214 model year 2016 Optima vehicles because the right front axle driveshaft may crack and fail, potentially causing the vehicle to stop moving or roll unexpectedly.
Fontaine is recalling 70 modified Peterbilt and Kenworth trucks because an improperly fitted steering shaft may fail, increasing crash risk.
Hallee is recalling about 1,000 Starlit Nights Mosquito Net Bed Canopies sold on Amazon.com due to entanglement and strangulation hazards.
Probity Cell is recalling about 230 Glion SmartScooter Model 100 units because the frame can break at the folding point, posing a fall hazard.
BMW is recalling one 2017 X3 xDrive 28i because improper welding on the electric power steering control unit may increase the risk of a fire.
Halcore Group is recalling 2016-2017 AEV Traumahawk ambulances because defective seat tracks may cause the attendant seat to move rapidly during a crash, increasing injury risk.