State
73,722 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 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Baxter Healthcare is recalling 5,940 bottles of Sevoflurane inhalation anesthetic because the product failed stability specifications.
Chiesi USA is recalling ZYFLO CR (zileuton) extended-release tablets because they failed to meet dissolution specifications. The recall affects 2,118 bottles distributed nationwide.
GE Healthcare is recalling Precision 500D X-ray systems because a CRT monitor fell off its wall mount due to product aging.
Synthetopes Inc is recalling Sn-Mertiatide Kits nationwide due to a lack of processing controls. The recall covers all lots remaining within their expiry date.
Geritrex, LLC is recalling Senna Syrup bottles due to reports of atypical odor and unpleasant taste.
Glenmark Pharmaceuticals is recalling Estradiol Vaginal Inserts because the plunger delivery system is not functioning properly.
Cardiocommand Inc. is recalling five units of its Transesophageal Cardiac Pacing and Recording System, Model 7A, due to possible corrosion of the battery contacts.
Conformis is recalling 183 iTotal Hip Replacement System stems nationwide due to a 3mm discrepancy between approved and manufactured neck/head lengths.
Synthetopes Inc. is recalling Sulfur Colloid Reaction Vials nationwide due to a lack of processing controls.
Synthetopes Inc is recalling 82 vials of Sn-DTPA Kit 10 mg nationwide due to a lack of processing controls.
B. Braun Medical Inc. is recalling 40,176 bags of Heparin Sodium in Dextrose because testing showed the drug had lower potency than required by USP specifications.
Philips is recalling Patient Information Center iX software because infusion pump data may be recorded at 100 times the actual rate.
Synthetopes Inc. is recalling Sn-DMSA solution vials nationwide due to a lack of processing controls. The product is not for direct injection.
Philips is recalling IntelliBridge Systems configured with comma decimal separators because infusion pump data may be recorded at 100 times the actual values.
Synthetopes Inc. is recalling Sn-Pyrophosphate Kits because of a lack of processing controls. The recall covers all lots remaining within their expiry dates.
Laird Superfood is recalling Performance Mushrooms because the label incorrectly lists 14 mg of Iron instead of the actual 14 mcg.
Fresenius Kabi USA, LLC is recalling 11,981 vials of Ondansetron Injection, USP, 40 mg / 20 mL, because the product failed impurities and degradation specifications.
Bausch & Lomb is recalling Lotemax ophthalmic gel because it failed stability specifications for viscosity. The recall covers 17,083 bottles distributed nationwide.
Home Meridian is recalling Copeland Corner Curio cabinets sold at Havertys due to tip-over and entrapment hazards that can cause injury.
Isuzu is recalling 2018-2020 FTR and Chevrolet 6500XD vehicles because a steering stopper bolt jam nut may loosen, increasing the turning radius and crash risk.
Farber Specialty Vehicles is recalling 2017 Ford F-550s with Whelen brake lights that may illuminate without the brake pedal being pressed, potentially confusing other drivers.
SVO Group is recalling 2017-2018 Ford E-350 and E-450 shuttle buses because backup camera images may reverse, increasing crash risk.
Farber Specialty Vehicles is recalling 2018 International 4300 SBA vehicles equipped with Whelen brake lights that may illuminate without the brake pedal being pressed.
Altec is recalling 2017-2018 aerial devices because fasteners securing the rotation bearing may break, potentially causing the pedestal to separate from the turntable.
Altec is recalling 328 vehicles due to non-DOT brake line fittings that may leak, causing the parking brake to drag and increasing crash risk.