State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Katadyn North America Foods is recalling 2,719 pounds of Spicy Sausage Pasta because the label lists beef but the product contains pork.
Yamaha is recalling about 875 model year 2015 YZ250FFL and YZ250FFW competition off-road motorcycles because the engine can lock up during operation, causing a crash.
Kiddie Korral is recalling pink hooded sweatshirts for children because the drawstrings pose a strangulation risk. Consumers should remove the drawstrings or return the items for a refund.
Giggles International is recalling about 13,000 Animated Sing-Along Monkey toys sold at Cracker Barrel because the battery compartment can overheat and cause burns.
Schneider Electric is recalling about 62,500 PowerPact J-frame circuit breakers because they may fail to trip during overloads, posing fire, burn, and shock risks.
Fresenius Kabi USA is recalling 101,200 vials of Midazolam Hydrochloride Injection due to potential glass fractures and particles that compromise sterility.
Nellcor Puritan Bennett is recalling 324 Puritan Bennett 980 Ventilators because a capacitor component can fail, causing a dim screen and thermal odor.
Fresenius Kabi USA is recalling 184,550 vials of Ondansetron Injection due to potential glass fractures and particles that compromise sterility.
TomoTherapy Incorporated is recalling 210 TomoTherapy Treatment Systems worldwide due to a software defect that may fail to monitor jaw position after an error, potentially leading to incorrect treatment delivery.
Ferrara is recalling 12 model year 2014 Fire Custom trucks because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.
PFM Medical is recalling ASEPT 600 ml Drainage Kits because they may exceed USP limits for bacterial endotoxin. The recall affects 1,470 units distributed in the US and abroad.
Fresenius Kabi USA is recalling 240,550 vials of Cyanocobalamin Injection due to potential glass fractures and particles that compromise sterility.
Siemens is recalling three Mammomat Inspiration systems because the workstation table may fall over if not secured, posing a risk of serious injury.
Smith & Nephew is recalling 45 units of the Legion COCR Constrained Femoral Component because the stem taper is undersized and the gauge point is not deep enough.
Medtronic MiniMed is recalling Silhouette and Sure-T infusion sets because tubing may detach, interrupting insulin delivery without an alarm.
Smith & Nephew is recalling 23 units of the Legion COCR Constrained Femoral Component because the stem taper is undersized and the gauge point is not deep enough.
Hospira Inc. is recalling Fentanyl Citrate Injection vials because improperly crimped flip-top seals may compromise sterility.
Blue Bird is recalling 2015-2016 Vision and All American school buses because a defective parking brake pedal assembly may fail to engage, increasing crash risk.
Siemens Medical Solutions is recalling 149 units of Syngo.plaza and syngo Imaging XS software because printouts may be in incorrect anatomical size, potentially influencing diagnostic decisions.
PFM Medical is recalling 75 units of Thoracentesis & Paracentesis Procedure Trays because they may exceed USP limits for bacterial endotoxin.
Baxter Healthcare is recalling 19,152 containers of Famotidine Injection 20 mg due to a complaint reporting the presence of plastic and rubber particulate matter.
Farber Specialty Vehicles is recalling 2005-2008 Winnebago WFG38S vehicles with specific Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.
PFM Medical is recalling 90 units of 6F x 60 cm Dual Lumen CT PICC catheters because they may exceed USP limits for bacterial endotoxin.
Invacare is recalling 5,963 Perfecto 2 V Oxygen Concentrators because defective sieve beds allow dust to migrate, reducing oxygen concentration.
Skeletal Dynamics is recalling 1,700 Align Radial Stems because a report was received indicating the device fractured.