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.
CAMP USA is recalling Cassin Blade Runner and Alpine crampons because the front part can break, posing a fall hazard. No injuries have been reported.
Synthes (USA) Products LLC is recalling 1,113 Sciatic Nerve Retractors due to a potential for micropores to form, which could allow fluid to enter the hollow handle.
Michael Foods is recalling Crystal Farms Shredded Hash Browns because the product may contain small slivers of shredded golf ball.
Winco Mfg. is recalling 27 Elite Care chairs because the foam used was not fire retardant as required.
Winco Mfg. is recalling 29 Inverness recliners because the foam was mislabeled as fire retardant but is actually standard foam.
C.R. Bard is recalling 534,972 Magic3 Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.
Wockhardt USA LLC is recalling 3,378 bottles of Lisinopril 20 mg tablets because an FDA inspection found inadequate investigations of past market complaints.
Veridex, LLC is recalling 1,560 Cell Search Circulating Tumor Kits due to the presence of artifacts and control failures.
Siemens Medical Solutions is recalling 586 Artis zee/zeego angiography systems because a system error could prevent users from exiting the X-ray locking function without a restart.
Winco Mfg., LLC is recalling Drop Arm Care Cliner chairs because the foam was mislabeled as fire retardant but is actually standard foam.
C.R. Bard is recalling 91,140 Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.
C.R. Bard is recalling 14,310 units of Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.
Medtronic is recalling EOPA Arterial Cannulas (Lot 2015060544) because they were shipped without the required guidewire.
International Biophysics Corp. is recalling 100 IBC Suction Wands because heat seals on sterile pouches may not meet strength criteria.
Trilliant Surgical Ltd. is recalling 102 units of non-sterile cannulated screw countersinks because their cutting efficiency was out of specification.
International Biophysics Corp. is recalling 771 IBC Vascular Loops because heat seals on sterile pouches may not meet strength criteria.
Wockhardt USA is recalling 1,704 bottles of Lisinopril 5 mg tablets because an FDA inspection found inadequate investigations of past market complaints.
Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Acetaminophen reagents due to a change in N-acetylcysteine concentration that may cause assay interference.
UCB, Inc. is recalling Univasc (moexipril HCl) tablets because they failed 24-month dissolution testing. The recall covers 2,916 bottles distributed nationwide.
C.R. Bard is recalling specific lots of Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.
C.R. Bard is recalling 37,686 Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters due to a potential breach of the sterile barrier packaging.
Cepheid is recalling Xpert CT/NG Urine Specimen Collection Kits because some lots contain a sub-component with an expiration date earlier than the kit's expiration date.
Cepheid is recalling Xpert CT/NG Vaginal/Endocervical Specimen Collection Kits because some lots contain a sub-component with an earlier expiration date than the kit itself.
Sun Pharma Global Fze is recalling 35,235 bottles of Bupropion Hydrochloride Extended-Release Tablets because they failed to meet drug release specifications during stability testing.
Spartan Motors is recalling 2012-2015 Gladiator and MetroStar emergency vehicles because front splay rails may crack and separate, risking cab collapse.