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.
Cabrinha is recalling about 2,900 kiteboard control systems because a stainless steel component can break, causing loss of kite control and posing injury and fall hazards.
Siemens is recalling 159 RAPIDPoint 500 Blood Gas Analyzers because a blank patient ID field may cause demographic errors.
PAR Sterile Products LLC is recalling Buprenorphine Hydrochloride Injection due to the presence of white, crystalline particulates in the vials.
CooperSurgical is recalling lnflatoball Latex Rubber Pessaries because the secondary packaging incorrectly states the product is latex-free, despite being made of 100% latex.
Stryker is recalling 65 PROFESS Registration Kits shipped near or past their expiration dates. The kits are used for intranasal and sinus surgery.
Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 7.5 mg, because they failed impurity specifications. The recall covers 6,138 bottles distributed nationwide and in Puerto Rico.
Sun Pharmaceutical Industries is recalling specific lots of Olanzapine Tablets, 2.5 mg, because they failed impurity specifications.
Almore International Inc. is recalling Microfil Composite Instruments because packaging labels incorrectly display a sterile symbol, although the devices are not sterile.
Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 20 mg, because they failed impurity specifications. The recall covers 14,784 bottles distributed nationwide and in Puerto Rico.
Teva Pharmaceuticals USA is recalling specific lots of Prednisolone Oral Solution because they failed stability specifications.
Akorn, Inc. is recalling 1,292 kits of IC-Green (indocyanine green for injection) due to low pH values. The product was distributed nationwide.
Sun Pharmaceutical Industries is recalling Olanzapine Tablets, 10 mg, because they failed impurity specifications. The recall covers 38,316 bottles distributed nationwide and in Puerto Rico.
Nova Bus is recalling 2016 LFS Artic transit buses because a network communication loss may cause the computer to apply full throttle without driver input.
PACCAR is recalling 2012-2018 Kenworth T800 and T880 trucks because an incorrectly sized brake control airline may increase stopping distance and crash risk.
Daytona Helmets International is recalling specific Skull Cap D1, D3, and D6 helmets manufactured in May 2015 because they may not adequately protect the wearer in a crash.
Bradshaw International is recalling Bialetti coffee presses because the glass beakers can break during normal use, posing a laceration hazard.
VanMoof is recalling B and S series bicycles because front fender bolts may not break during obstructions, posing fall and impact hazards.
Hickory Springs is recalling Summit-brand seat covers for RAM ProMaster, Ford Transit, and Mercedes Sprinter vehicles because the seam may prevent seat-mounted air bags from deploying.
Forest River is recalling 2018 Palomino recreational trailers because the Federal Placard lists incorrect tire and rim specifications, which may increase crash risk.
Terex is recalling 2007-2016 aerial devices and digger derricks because the onboard electrical breaker may fail to trip during a short circuit, increasing the risk of user injury.
Terex is recalling 444 Digger Derricks and Aerial Devices from 2012-2017 because a hood switch may prevent remote engine shutdown, increasing injury risk.
Valley Innovative Services is recalling approximately 130,071 pounds of frozen entrée products containing waffles due to possible Listeria monocytogenes contamination.
Honeywell is recalling SWIFT wireless gateways sold with fire alarm systems because they may fail to communicate with detectors during a fire, leaving occupants unalerted.
Bombardier is recalling 2017 Can-Am Spyder RT motorcycles because a manufacturing error may cause headlights to shine too high, potentially blinding oncoming traffic.
Keystone RV Company is recalling 2017-2018 Raptor fifth-wheel recreational trailers because tires may contact outriggers, risking tire damage and loss of control.