State
73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Fougera Pharmaceuticals is recalling 14,665 tubes of Desonide Ointment because unit boxes may contain tubes labeled as Ketoconazole Cream.
BioMerieux SA is recalling ETEST Cephalothin CE 256 Foam packaging because current shelf-life claims are not supported by internal testing.
Zimmer Biomet is recalling Orthosize Templating Version 1.2.6 digital templates because they were created with incorrect files, affecting preoperative planning for orthopedic surgery.
BioMerieux SA is recalling ETEST Gentamicin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
Sun Pharmaceutical Industries, Inc. is recalling 83,188 vials of Testosterone Cypionate Injection due to the presence of particulate matter.
BioMerieux SA is recalling ETEST Doripenem DOR32 FOAM packaging strips because internal testing does not support the current shelf-life claims.
Tearscience is recalling LipiFlow Thermal Pulsation Systems because the labeled storage temperature does not match tested conditions for the full shelf life.
BioMerieux SA is recalling ETEST Imipenem IP32 Foam packaging because the current shelf-life claims are not supported by internal testing.
Vygon MFG is recalling 30,700 AMS-636 Microbore extension sets because the package displays an incorrect priming volume.
BioMerieux SA is recalling ETEST Tobramycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
BioMerieux SA is recalling ETEST Vancomycin antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
BioMerieux SA is recalling Etest Benzyl Penicillin PG256 FOAM packaging because shelf-life claims are not supported by internal testing.
BioMerieux SA is recalling ETEST Ciprofloxacin CI 32 Foam products because their shelf-life claims are not supported by internal testing.
AvKARE Inc. is recalling 116 cartons of 500 mg Famciclovir tablets because the product exceeded specifications for unknown impurities.
BioMerieux SA is recalling ETEST Ceftriaxone antimicrobial susceptibility testing strips because their shelf-life claims are not supported by internal testing.
Teleflex Medical is recalling 7,600 units of Green Non-Latex Robertazzi Nasopharyngeal Airways due to a labeling error. The voluntary recall covers products distributed in the US, Canada, and Mexico.
Pfizer is recalling specific lots of Quillivant XR extended-release oral suspension because the product failed to meet dissolution specifications at 12 months.
Pfizer is recalling Quillivant XR extended-release oral suspension due to failed dissolution specifications at 12 months.
Pfizer is recalling Quillivant XR extended-release oral suspension because it failed to meet dissolution specifications at 12 months. The recall affects 28,938 units distributed nationwide.
Schwarze is recalling 2013-2017 street sweepers because incorrect air brake fittings may cause air leaks and unexpected vehicle stops.
Look Cycle is recalling about 800 road bikes and Aerostems because a stainless steel clamp can corrode and break, posing a fall and crash hazard.
Hyundai is recalling 2017 Elantra vehicles because a damaged steering connector may cause loss of power steering assist, increasing crash risk.
SolarWorld is recalling about 97,000 solar panel connectors sold in the U.S. because microscopic cracks can allow moisture to leak in, posing an electrical shock hazard.
Ford is recalling 2017 Edge vehicles with Panoramic Vista Roofs due to an improperly welded windshield header that reduces lateral structural integrity.
Ford is recalling 2017 F-450 and F-550 Superduty trucks because the driveline may vibrate and fracture at highway speeds, potentially causing loss of motive power and increasing crash risk.