State
73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Synthes USA HQ, Inc. is recalling 374 Soft Tissue Retractors because the locking screw nut may break if overtightened.
GE Healthcare is recalling 710 Vivid E9 ultrasound systems worldwide due to a software defect that can cause the system to slow down and lock up during critical procedures.
Stryker is recalling Model FL14E Rose Beds because siderails may appear latched when they are not, posing a risk of patient injury.
GE Healthcare is recalling four models of nuclear medicine and CT imaging systems because the detector may contact a patient's elbow during specific SPECT scans.
American Beverage Corp. is recalling Big Burst Fruit Punch Drink because the sports cap nozzle may dislodge and be ingested, posing a health hazard.
American Beverage Corp is recalling Guzzler Kiwi-Strawberry beverages because a part of the nozzle cap may dislodge and be ingested.
American Beverage Corp. is recalling Big Hug Fruit Barrel Blue Raspberry bottles due to a potential choking hazard from the sports cap.
Ergosafe Products LLC is recalling 233 Medcare Max-500 patient stands because the lift mechanism might fail under the labeled 500-lb load rating.
American Beverage Corp is recalling Big Hug Lemonade Fruit Drink because a part of the nozzle cap could become dislodged and ingested, posing a health hazard.
American Beverage Corp. is recalling Big Burst Citrus Punch Drink bottles due to a potential choking hazard from the sports cap nozzle.
Philips is recalling nine Brilliance iCT CT scanners because the footrest extension can contact the gantry or user during operation.
American Beverage Corp. is recalling Big Hug Lemon Lime Fruit Drink bottles due to a risk that nozzle cap parts could be ingested after excessive chewing.
GE Healthcare is recalling Centricity Laboratory System software versions 3.3, 4.0, and 4.1 because panel reflexing may fail under specific conditions.
American Beverage Corp. is recalling Big Burst Blue Raspberry Drink because the sports cap nozzle may dislodge and be ingested if chewed excessively.
American Beverage Corp. is recalling Big Hug Fruit Barrel Kiwi Strawberry bottles due to a potential choking hazard from dislodged nozzle cap parts.
American Beverage Corp is recalling Guzzler Lemonade 20 fl. oz. bottles due to a risk that nozzle cap parts may dislodge and be ingested.
Olympus America Inc. is recalling 263 Endoscopic Flushing Pumps because the pump head may not be locked, potentially causing the device to stop and enter power stand-by mode during procedures.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry CK Slides due to slide dispense issues. The recall affects 86,503 units distributed worldwide.
Siemens Healthcare Diagnostics is recalling ADVIA 1650 system software due to incorrect ration parameter flagging behavior.
American Beverage Corp. is recalling Big Burst Lemon Lime Drink bottles due to a potential choking hazard from dislodged nozzle cap parts.
Spacelabs Healthcare is recalling 54 qube Compact Patient Monitors because an incorrect microcontroller may prevent the device from powering on.
American Beverage Corp. is recalling Big Burst Orange Drink in 16 oz PET bottles because the nozzle cap may dislodge and be ingested.
American Beverage Corp is recalling Big Juicy Grape Drink because the sports cap nozzle may dislodge and be ingested. The firm does not anticipate finding impacted product in the market.
American Beverage Corp is recalling Guzzler Alpine Freeze bottles because the sports cap nozzle may dislodge if chewed, posing a choking or ingestion risk.
Biomet, Inc. is recalling 25 units of Juggerknotless Drill Bits because the design may make it difficult to insert the suture anchor into the bone.