State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Far East Brokers is recalling about 6,000 children's chairs and swings because the screen-printing contains excessive lead, violating federal standards. No injuries have been reported.
Southeast Toyota Distributors is recalling 2015-2016 Toyota and Scion vehicles because the load carrying capacity label may be incorrect, potentially leading to vehicle overload.
Volkswagen Group of America is recalling 2007-2009 Audi A8 and S8 vehicles because the sunroof glass may not be properly secured and could detach while driving.
Akorn, Inc. is recalling specific lots of Sulfacetamide Sodium Ophthalmic Solution because they failed antimicrobial effectiveness testing, raising concerns about sterility.
Invisiblu International LLC is recalling LGD-Xtreme capsules containing unapproved ligandrol because the product was marketed without an approved NDA or ANDA.
FDA is recalling Curity All Purpose Sponges due to compromised sterility from a barrier breach. The recall affects units distributed in the US and 20 other countries.
Covidien LLC is recalling Vistec X-Ray Detectable Sponges because a breach of the barrier packaging may have compromised sterility.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
Covidien LLC is recalling Curity Gauze Sponges because a breach of the barrier packaging may have compromised their sterility.
Forest River is recalling 2015 Glaval Synergy transit buses because steering boxes may wear prematurely, risking loss of steering control.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
Newmar is recalling 2014-2016 Dutch Star motorhomes because a defective steering box may cause loss of steering control.
Terex Advance is recalling 338 model year 2016 Front Discharge Concrete Mixer trucks because a weld failure could cause the main chute to detach while driving, increasing crash risk.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges because a breach of the barrier packaging may have compromised their sterility.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility caused by a breach of the barrier.
Pentax Medical is recalling 423 Video Duodenoscopes nationwide after reports of carbapenem-resistant Enterobacteriaceae (CRE) infection at a medical facility.
FDA is recalling Kerlix X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
The FDA is recalling Kerlix X-Ray Detectable Laparotomy Sponges due to compromised sterility from a barrier breach.
The FDA is recalling Curity X-Ray Detectable Laparotomy Sponges due to compromised sterility caused by a barrier breach.
The FDA is recalling Vistec X-Ray Detectable Sponges because a breach in the packaging barrier may have compromised their sterility.
Crossroads is recalling 2016-2017 Hill Country and Sunset Trail trailers because opening the outside kitchen door may extinguish inside burners, allowing propane to build up and potentially cause a fire or explosion.
Windstone Medical Packaging is recalling specific Laparotomy Packs because the included Medtronic Kerlix sponges may have compromised sterile barriers.
ConMed is recalling 991 Hip Preservation System PreBent Burs because an assembly error caused metal shavings to be released during use.
Elekta is recalling Monaco RTP System software versions 5.10.00 and higher because a specific export setting causes incorrect jaw positioning in radiation therapy plans.