State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
U.B.C Food Distributors, LLC is voluntarily recalling strawberry and mango flavored gelatin mixes because they contain undeclared food dyes.
Beckman Coulter is recalling Access 2 Immunoassay Systems because the Small Form Factor Console PC may experience an 'MFC Exception' error during normal operation.
Straumann USA is recalling 111 units of Bone Level Implants because the product transfer piece was fitted with a Narrow Connect instead of a Regular Connect.
U.B.C Food Distributors is voluntarily recalling strawberry and mango flavored gelatin mixes because they contain undeclared food dyes.
Pharmaceutical Associates Inc. is recalling 9,640 unit dose cups of Cyproheptadine HCl Syrup because an unidentified impurity exceeded specifications during stability testing.
Smiths Medical is recalling a specific lot of CADD-Solis Medication Safety Software Administrator CDs because they were shipped with incorrect software loaded.
Obagi Medical Products is recalling 975 bottles of Obagi Nu-Derm Clear due to a labeling mix-up where Exfoderm Forte contents were shipped.
Merit Medical Systems is recalling 56 Maestro Microcatheters because they were packaged with a 2.8 F distal tip instead of the labeled 2.4 F.
Siemens Healthcare Diagnostics is recalling Calibrator E kits due to positive bias in Cortisol and Progesterone assays on ADVIA Centaur Systems.
Apotex Inc. is recalling specific lots of Candesartan Cilexetil Tablets because they failed impurity and degradation specifications.
Apotex Inc. is recalling Candesartan Cilexetil Tablets, 16 mg, because out-of-specification results were observed for specific impurities and total impurities.
Pfizer is recalling 16,000 TORISEL kits because impurities in the diluent may cause crystals to form after cold storage. The TORISEL drug vials are not affected.
Apotex Inc. is recalling Candesartan Cilexetil Tablets, 32 mg, because out-of-specification results were observed for specific impurities and total impurities.
Physicians Total Care is recalling specific lots of Loratadine 24 HR-OTC 10 mg tablets because they may contain chipped or broken pieces.
PACCAR is recalling 2015 Kenworth heavy trucks because an undersized wire in the instrument panel harness may overheat, increasing the risk of a vehicle fire.
Daimler is recalling 2014-2015 Freightliner trucks because defective air brake valves may reduce braking performance and increase crash risk.
General Motors is recalling 2015 Chevrolet and GMC vehicles because a steering module defect may cause sudden loss of power assist, increasing crash risk.
McDonald's is recalling Hello Kitty Birthday Lollipop Whistles because internal components can detach, posing choking and aspiration risks to young children.
Sutphen is recalling 2000-2014 aerial devices because a cable failure could cause the ladder to collapse, increasing injury risk.
BMW is recalling 2015 MINI Cooper Hardtop 2 Door vehicles because the seatback adjustment mechanism may not be fully engaged, increasing injury risk in a rear impact.
Forest River is recalling 2015 Wildwood and Salem Ice Cabin trailers because the draw bar may break, potentially causing the trailer to detach from the vehicle.
PACCAR is recalling specific 2014-2015 Kenworth and Peterbilt trucks because defective parking brake valves may reduce braking performance and increase crash risk.
Toyota is recalling 2014 Camry and Avalon vehicles because a front suspension part may separate, increasing the risk of a crash.
Dynamic Tire Corp. is recalling specific Towmax STR tires with incorrect load and pressure markings that could lead to overinflation and tire failure.
Ford is recalling 2014 F-150 and Flex vehicles because a seat defect may cause the passenger airbag to fail to deploy in a crash.