State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Newmar is recalling 2016-2018 Mountain Aire motorhomes because the DEF tank bracket may contact the tag axle tire, potentially causing tire failure and increasing crash risk.
Altec Industries is recalling 2014-2017 Flatbed Bodies with stake rails because the rails may become dislodged, increasing the risk of injury or a crash.
Hyundai is recalling 2018 Genesis G80 and G90 vehicles because incorrect primer may reduce windshield and rear window bonding strength, increasing crash risk.
General Motors is recalling 2016-2018 Chevrolet Cruze LS vehicles because they may leak gasoline after a rear-impact crash and rollover, increasing fire risk.
ALDI is recalling Ambiano mini deep fryers because the heating element can overheat, posing fire and burn hazards. Three fire incidents and minor property damage have been reported.
Keystone RV Company is recalling 2016-2017 Crossroads Redwood travel trailers because a rear ladder may block the secondary emergency exit window, increasing injury risk.
Munchkin is recalling Waterpede bath toys because they can break apart and expose small beads, posing a choking hazard to young children.
Tobi USA LLC is recalling Babynest crib bumpers sold online at babybay.us because the strings pose a strangulation hazard to babies.
illy is recalling about 65,000 8.8-ounce whole bean coffee cans because the lid can detach suddenly with force upon opening, posing an injury hazard.
Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder (Kratom) because it may be contaminated with Salmonella.
Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder (Green Horn) sold as Herbal-Salvation.com due to potential Salmonella contamination.
AuroMedics Pharma LLC is recalling Linezolid Injection bags due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.
AuroMedics Pharma LLC is recalling 261,250 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
AuroMedics Pharma LLC is recalling 308,112 bags of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of mold.
Philips is recalling 184 MultiDim Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
Philips is recalling 37 MultiDiagnost Eleva imaging systems because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
AuroMedics Pharma LLC is recalling Levetiracetam Injection due to a lack of assurance of sterility and a confirmed report of leaking bags and mold.
Philips is recalling 199 MD-Eleva imaging systems because a tilt actuator may break, causing the table to rotate uncontrollably at high speed.
Philips is recalling 206 MD-Eleva imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.
Zimmer Biomet is recalling 18 modular hip head components because two lots of different sizes were potentially commingled. This may lead to the use of an incorrect sized head.
Sanofi-Aventis is recalling 19,580 vials of Docetaxel injection concentrate due to potential over-concentration. The affected lots were distributed nationwide.
AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and a confirmed report of leaking bags with mold.
AuroMedics Pharma LLC is recalling 67,300 bags of Levetiracetam Injection due to a confirmed report of leaking bags and mold found between the outer bag and overwrap.
Philips is recalling the MultiDiagnostic-Eleva imaging system because a broken actuator fixation can cause the patient table to rotate uncontrollably at high speed.
AuroMedics Pharma LLC is recalling specific lots of Levofloxacin in 5% Dextrose Injection due to a lack of assurance of sterility and reports of leaking bags with mold.