State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Excelsior Medical Corp is recalling specific lots of Heparin Lock Flush syringes because they failed potency testing.
Navilyst Medical is recalling 10 BioFlo Hybrid PICC catheter kits manufactured before July 15, 2014, because they lack a specification change that reduces hemolysis during blood sampling.
Physio-Control is recalling LIFEPAK 15 monitor/defibrillators with the EtCO2 feature because the respiratory rate display may obscure the leading digit of the EtCO2 value.
Valeant Pharmaceuticals is recalling 3,827 bottles of Lodrane D capsules because the outer cartons were mislabeled with the wrong active ingredient.
FSC Laboratories is recalling 1,435 Flexichamber Anti-Static Valved Collapsible Holding Chambers because the seal around the mouthpiece was torn or loose.
Nostrum Laboratories is recalling Nitrofurantoin Oral Suspension because it failed to meet dissolution specifications. The recall covers 2,839 bottles distributed nationwide.
Par Pharmaceutical is recalling Pramipexole Dihydrochloride Extended Release tablets because they contain a known impurity above approved specification levels.
Navilyst Medical is recalling BioFlo PICC catheters manufactured before July 15, 2014, because they lack a specification change that reduces hemolysis during blood sampling.
Valeant Pharmaceuticals is recalling specific lots of Chlordiazepoxide HCl/Clidinium Bromide capsules because they failed impurities and degradation specifications.
Navilyst Medical is recalling 357 Xcela Hybrid PICC catheters manufactured before July 15, 2014, because they lack a specification change that reduces hemolysis during blood sampling.
Navilyst Medical is recalling specific BioFlo and Xcela PICC catheters because they lack a manufacturing change that reduces hemolysis during blood sampling.
Natus Medical is recalling 13,541 neoBLUE Phototherapy systems to add a warning statement to the instructions and provide a laminated Quick Guide for each device.
Galderma Laboratories is recalling Doxycycline USP Capsules 40 mg because some bottles are missing lot numbers or expiration dates.
Valeant Pharmaceuticals is recalling specific lots of Librax capsules because they failed impurity and degradation specifications.
Leica Biosystems Richmond Inc. is recalling 33 Ariol automated scanning microscope systems because a manufacturing error resulted in an improperly activated Windows 7 operating system.
Sandoz Inc is recalling 3,048 bottles of Lisinopril Tablets USP, 30 mg, because the package insert is incorrect or missing.
Forest River is recalling 2016-2017 Flagstaff and Work N' Play trailers because a propane regulator sight glass may crack, allowing gas to leak and potentially cause a fire.
Navistar is recalling 2016 IC Bus RE school buses because child seats may separate from the base frame due to bolt failure, increasing injury risk in a crash.
Mayborn USA is recalling about 255,000 Tommee Tippee electric bottle and food warmers due to a fire hazard. The units can overheat, melt, smoke, and catch fire.
The Land of Nod is recalling Octo-rattles because fabric discs on the tentacles can detach, posing a choking hazard to young children.
General Motors is recalling specific 2016 Chevrolet Equinox and GMC Terrain vehicles because their certification labels may display incorrect tire and rim size information.
Gillig is recalling 112 model year 2012-2016 Low Floor vehicles because the rear brake lights may flash inadvertently, which could confuse other drivers and increase crash risk.
Navistar is recalling 1,191 model year 2017 International trucks because an electrical short in the engine control module can cause the engine to stall without restarting.
Spartan Motors is recalling 2004-2016 Gladiator aerial emergency vehicles because air brake timing issues may increase stopping distance and crash risk.
Eldorado is recalling 2016 Aerotech, Aero Elite, and Advantage shuttle buses because a component in the electrical power distribution center may break, causing electrical arcing and increasing the risk of fire.