State
73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
GE Healthcare is recalling 123 Lunar iDXA Advance bone densitometers because a control panel issue may cause the start button to stick, potentially leading to accidental radiation exposure.
Welch Allyn is recalling ELI PC Service software because it may not meet defibrillation withstand safety requirements for medical electrical equipment.
Uromedica Inc. is recalling 11 ProACT Implantation Instrument Sets because defective U-channel sheaths may damage ProACT implant devices during use.
GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel defect may cause the start button to stick, potentially leading to accidental radiation exposure.
Kerr/Pentron is recalling 111 trial kits of Nexus Universal with OptiBond Universal due to a packaging error that included the incorrect bonding agent, potentially increasing the risk of bond failures.
Beckman Coulter is recalling SYNCHRON Systems Barbiturates Reagent because cross-reactivity testing may not meet claims, potentially causing false positive or negative results.
Welch Allyn is recalling 78,521 Surveyor S12 and S19 bedside monitors and patient cables because they may not meet defibrillation withstand safety requirements.
ICU Medical is recalling 83 Cogent Hemodynamic Monitoring Systems due to software issues that may cause inaccurate data, unit shutdown, or loss of display.
Welch Allyn is recalling 78,521 Q-Tel RMS systems because they may not meet defibrillation withstand safety requirements.
GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel defect may cause the start button to stick, potentially leading to accidental radiation exposure.
Welch Allyn is recalling 78,521 ECG lead sets because they may not meet defibrillation withstand safety requirements.
Welch Allyn is recalling T12 wireless ECG devices because they may not meet defibrillation withstand safety requirements.
Elekta Inc is recalling 25 Leksell Vantage Stereotactic System Instrument Carriers because a faulty locking piece may not meet required locking force standards.
Welch Allyn is recalling S4 Wireless Telemeters and patient cables because they may not meet defibrillation withstand safety standards.
Welch Allyn is recalling Q-Stress and XScribe diagnostic devices because they may not meet specific defibrillation withstand safety requirements.
U&I Corp. is recalling 42 Velofix SA cervical cages because screw-hole dimensions may be out of range, posing a risk of screw pullout or instability.
Avanos Medical is recalling CORFLO Percutaneous Endoscopic Gastrostomy (PEG) Kits because the tube may become blocked at the adapter, potentially delaying or aborting procedures.
GE Healthcare is recalling 123 Lunar iDXA bone densitometers because a control panel issue may cause the start button to stick, potentially leading to accidental radiation exposure.
Welch Allyn is recalling 78,521 lead diagnostic electrocardiographs because they may not meet defibrillation withstand requirements.
Welch Allyn is recalling H12+ Holter Recorders and patient cables because they may not meet defibrillation withstand requirements.
Smiths Medical ASD Inc. is recalling 100 units of Portex Lumbar Puncture Trays because the inner trays were mislabeled with an incorrect model number.
Siemens is recalling Atellica CH 930 Analyzers with specific software versions due to a defect that may cause incorrect test results.
Bio-Rad Labs is recalling 376 units of the Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test, Lot 18200A, due to elevated lot-to-lot bias affecting antibody measurements.
Obalon Therapeutics is recalling 45 Obalon Balloon Systems because the touchscreen may lose calibration, preventing balloon inflation.
Boston Scientific is recalling MoXy Laser Fibers to update instructions and reduce the likelihood of metal cap and fiber tip breakage.