State
73,718 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 73,718 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Alliance Tire is recalling specific Galaxy DH241-G commercial truck tires because improper vulcanization may allow the tread to separate from the casing, increasing crash risk.
Keystone RV is recalling 2020 Crossroads trailers because improper WiFi wiring circuit protection may increase the risk of fire during a short circuit.
Chrysler is recalling 2014-2019 Ram ProMaster vans because the transmission shifter cable may disconnect, causing unintended vehicle movement and crash risk.
General Motors is recalling 2014-2015 Cadillac CTS-V Sport vehicles because rear-axle differential roll pins may fracture, potentially causing the driver to lose control.
Mitsubishi is recalling 1998-2000 Montero vehicles because air bag inflators may rupture or underinflate in a crash, increasing injury risk.
Rosenbauer America is recalling 2014-2019 Commander vehicles because front shocks may separate, potentially damaging the steering gear and causing a loss of power steering assist.
PCNA is recalling approximately 5,000 Spare 10,000 mAh Power Banks because the lithium-ion batteries can overheat and ignite, posing fire and burn hazards.
General Motors is recalling 2003-2004 Pontiac Vibe vehicles because the front passenger air bag may not inflate properly in high temperatures, increasing injury risk.
STIHL is recalling RE 90 pressure washers because the nozzle can detach from the spray wand under pressure, posing an injury risk.
Varidesk is recalling Stand2Learn stools because the foot support bars can break, posing a fall hazard. No injuries have been reported.
Hikma Pharmaceuticals is recalling specific lots of Ketorolac Tromethamine Injection because of the presence of polydimethylsiloxane particles.
Assurance Infusion is recalling BUP 21MG/CLON 252MCG/MORP 20MG/ML Injection syringes due to a lack of sterility assurance. The recall covers products distributed nationwide.
Assurance Infusion is recalling specific lots of Hydromorphone 3mg/mL injection syringes due to a lack of sterility assurance. The products were distributed nationwide.
Assurance Infusion is recalling specific lots of Morphine 30mg/mL injection syringes due to a lack of sterility assurance. The affected products were distributed nationwide.
Assurance Infusion is recalling specific lots of a multi-drug injection syringe due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Baclofen injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling two syringes of Phenol 2.5% Sterile Solution because of a lack of sterility assurance.
Assurance Infusion is recalling specific syringes containing a combination of drugs due to a lack of sterility assurance.
Assurance Infusion is recalling 166 vials of Testosterone Cypionate 200mg/mL oil injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling 20 mL syringes of BUP 15MG/CLON 300MCG/FENT 1500MCG/ML injection due to a lack of sterility assurance.
Assurance Infusion is recalling BUP 3 mg/MORP 15 mg/mL Injection syringes due to a lack of sterility assurance. The recall covers specific lots distributed nationwide.
Assurance Infusion is recalling specific lots of Buprenorphine and Fentanyl injection due to a lack of sterility assurance.
Assurance Infusion is recalling specific lots of Morphine 7mg/mL injection syringes due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling specific lots of Buprenorphine and Morphine injection due to a lack of sterility assurance. The product was distributed nationwide.
Assurance Infusion is recalling Bi-Mix Forte 30 mg/2 mg/mL injections because of a lack of sterility assurance. The affected lot was distributed nationwide.