State
73,486 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.
Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,486 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Olympus Corporation issued updated reprocessing instructions for the BF-XP60 bronchofiberscope to align with FDA 2015 guidance on medical device reprocessing validation and labeling.
Shyft Group is recalling certain 2020-2022 Spartan K1 and K2 RV chassis because rear suspension fasteners may not have been tightened properly, which could allow the rear axle to shift and increase crash risk. Free repair is available.
Peach Cargo is recalling 2021-2022 Cargo Trailers because improperly tightened spindle nuts may cause axle vibration and overheating, increasing crash risk.
Nissan is recalling certain 2014-2017 hybrid SUVs because software may shut down the engine, causing a loss of drive power and increasing crash risk.
Arcimoto is recalling TRiO conversion kits because a connecting bolt may fail, causing immediate loss of traction power and increasing crash risk.
Ford is recalling certain 2021 Bronco vehicles because the passenger air bag vent may open prematurely during deployment, increasing the risk of injury during a crash.
Mercedes-Benz is recalling 2020 GLS 580 vehicles because incorrect air bag control software may cause the driver's air bag to deploy improperly, increasing injury risk.
Micro Bird is recalling 2022 G5 school buses because misaligned wheels can cause uneven tire wear and increase crash risk. Dealers will re-align the wheels free of charge.
Micro Bird is recalling one 2022 G5 transit bus because an incorrectly installed alignment ring can cause wheel misalignment, increasing crash risk.
Volvo is recalling 2001-2009 S60 and 2001-2006 S80 vehicles because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.
Jayco is recalling 2021-2022 Flight SLX travel trailers because the cooktop may not be sealed from the furnace, creating a fire risk.
Highland Ridge RV is recalling 2021 Open Range recreational trailers because the cooktop cabinet may not be sealed from the furnace, creating a fire risk.
Starcraft is recalling 2021-2022 Autumn Ridge Outfitter recreational trailers because the cooktop may invert during furnace operation, increasing fire risk. Dealers will install sealant and plywood panels free of charge.
Ford is recalling 2020-2021 Ranger Super Cab vehicles because fixed head restraints may interfere with child seat installation and anchor attachment.
Ultrasound gels sold under multiple brand names have been recalled due to potential bacterial contamination. Approximately 100,114 units distributed nationwide between August 2018 and August 2021 are affected.
Eco-Med Pharmaceutical, Inc. is recalling ultrasound gels and lotions that may contain bacterial contamination. Products were distributed nationally and internationally.
DuPont Nutrition USA is recalling Avicel RC-591 NF bulk powder (lot #2173766940) due to out-of-specification microbial contamination. The product was distributed as a component in finished drug formulations nationwide.
Glenmark Pharmaceuticals is recalling Fulvestrant Injection 250 mg/5 mL due to lack of assurance of sterility. The affected product was distributed nationwide in 28,658 cartons across multiple lots.
Glenmark Pharmaceuticals is recalling Arformoterol Tartrate Inhalation Solution 15 mcg/2 mL nationwide because the manufacturer lacks assurance of sterility for affected lots.
Phe Inc is recalling X Rated Honey For Men packets nationwide because the product contains Tadalafil and was marketed without FDA approval. Consumers should stop use immediately.
Aesculap Implant Systems is recalling Univation X System knee implant devices because they may loosen, potentially requiring revision surgery. All lots distributed in the US are affected.
C.R. Bard Inc is recalling approximately 4830 SureStep Foley catheter trays due to potential packaging defects that could compromise the sterile barrier.
Aesculap Implant Systems recalls Univation X System knee implants nationwide due to risk of loosening that could require revision surgery. All lots are affected.
Siemens SOMATOM CT systems with certain software versions may experience sporadic errors causing workflow interruptions and diagnostic delays. Affected systems should be updated to prevent scan aborts and patient rescans.
C.R. Bard Inc is recalling SureStep Foley Catheter Trays due to potential packaging defects that may compromise the sterile barrier. The affected lot includes 1140 units distributed nationwide.