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.
Genzyme Corporation is recalling specific lots of Thyrogen (thyrotropin alfa) because glass particles were found in the product after reconstitution.
Dole Fresh Vegetables Inc is withdrawing all salads produced at its Springfield, Ohio facility, including Dole and private label brands, due to a suspension of operations.
Dole is withdrawing all salads produced at its Springfield, Ohio facility. Consumers should identify products by a code starting with 'A' and stop using them.
Dole is withdrawing all salads produced in Springfield, Ohio, to suspend operations at the facility. Consumers should identify affected products by a code starting with 'A'.
Dole is withdrawing all salads produced at its Springfield, Ohio facility due to a safety concern. Consumers should check for specific product codes.
Dole is withdrawing all salads produced at its Springfield, Ohio facility, including Dole and private label brands, due to a safety issue.
Dole Fresh Vegetables Inc is withdrawing all Dole and private label salads produced at its Springfield, Ohio facility. Consumers should identify affected products by a code beginning with the letter A.
Mako Surgical Corporation is recalling 146 units of the Restoris Multicompartmental Knee System because damaged packaging may have compromised the sterile barrier.
Orscheln is recalling specific parking brake cable connector clips that may fail, potentially causing the vehicle to roll and increasing crash risk.
Cook Inc. is recalling 134 Kopans Breast Lesion Localization Needles because they may have been exposed to body fluids during processing, posing a potential risk of blood-borne pathogen transmission.
Philips is recalling 427 BrightView XCT gamma cameras because the collimator may contact the patient pallet or the gantry may halt prematurely during scans.
Baxter Healthcare is recalling 0.9% Sodium Chloride Irrigation bottles due to a product complaint identifying an insect as particulate matter.
Ivoclar Vivadent is recalling Helioseal Clear dental sealant because a production error may prevent the material from curing properly under specific lights.
KYMCO is recalling about 1,700 utility vehicles because the throttle can fail to return to idle, posing crash and injury hazards. No injuries have been reported.
ConvaTec is recalling Opti-Mist and Opti-Mist Clear nebulizer masks because a component defect reduces or stops aerosol output, potentially preventing patients from receiving medication.
Philips Medical Systems is recalling 117 BrightView X gamma cameras worldwide due to potential gantry motion halts and collimator contact with the patient pallet.
Z Gallerie is recalling Golda wall clocks because defective battery springs can cause batteries to overheat, posing a fire hazard.
Philips Medical Systems is recalling 677 BrightView gamma cameras because the collimator may contact the patient pallet or the gantry may halt prematurely during scans.
Aesculap Inc. is recalling 1,232 units of Columbus Revision and EnduRo Knee System packaging labeled as cementless, which are indicated for use with bone cement only.
Sun Pharma Global Fze is recalling specific lots of Alendronate Sodium Tablets 70 mg because unknown impurity levels exceeded specifications during stability testing.
Novadaq is recalling 110 PINPOINT Endoscopic Fluorescence Imaging Systems because the operator's manual lacks validated sterilization parameters for specific components.
Stryker is recalling AccuPlace Drace Stereotaxic Needle Guides because packaging defects may breach sterility. The recall covers 5,800 units distributed nationwide.
Stryker is recalling AccuPlace Round Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.
Volcano Corporation is recalling R-100 Sterile Equipment Covers because the outer shipping boxes may display incorrect expiry dates, although the inner product is correctly labeled.
Stryker is recalling AccuPlace Straight Level Needle Guides because packaging defects may compromise sterility. The recall affects 5,800 units distributed nationwide.