State

US Virgin Islands product recalls

73,388 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 39
Most recent: 2026-09-23

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20976–21000 of 73565

HighFDA (Devices)·Z-0988-2022·2022-04-27
Gallant DR Implantable Cardioverter Defibrillator Bluetooth Malfunction Affects Remote Monitoring
St. Jude Medical's Gallant DR implantable cardioverter defibrillator has a Bluetooth malfunction preventing remote monitoring and reducing battery life. The device enters inductive-only telemetry mode, requiring in-clinic monitoring instead.
Product
Gallant DR Implantable Cardioverter Defibrillator REF # CDDRA500Q
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0973-2022·2022-04-27
Artis zeego X-ray imaging system recalled for insufficient cooling
Siemens is recalling 183 Artis zeego X-ray imaging systems due to a cooling system defect that may prevent adequate X-ray tube cooling, triggering automatic system shutdown.
Product
Artis zeego, Model Number 10280959
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0774-2022·2022-04-27
Injectable Rifampin Recalled Due to Failed Quality Specifications
Mylan Pharmaceuticals is recalling injectable Rifampin vials nationwide due to failed impurities and degradation specifications discovered during stability testing.
Product
RIFAMPIN — RIFAMPIN (RIFAMPIN)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V282000·2022-04-27
Commercial buses with inoperative collision system lack required warning label
Navistar is recalling certain 2022-2023 commercial buses equipped without forward radar units. The required warning label indicating the collision mitigation system is inoperative may be missing, increasing crash risk.
Product
INTERNATIONAL — INTERNATIONAL, IC BUS HV, MV, RE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0975-2022·2022-04-27
X-ray Imaging System Coolant Deficiency May Disable Equipment Operation
The Artis Q X-ray system may fail to adequately cool the X-ray tube if coolant levels drop, causing the system to disable imaging and display error messages. 418 systems are affected nationwide.
Product
Artis Q ceiling, Model Number 10848281
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0963-2022·2022-04-27
Sight OLO Blood Analysis Device: Incorrect Reference Ranges May Display
The Sight OLO blood analysis device may display and print incorrect reference ranges in software versions 2.59.3 and earlier. This could occur when custom reference ranges were configured after device installation.
Product
The Sight OLO device is a computer vision based platform for blood analysis. The platform combines computer-vision algorithms for image processing to identify and quantify blood components (e.g., red blood cells) and their characteristics (e.g., cell volume) in an automated…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V279000·2022-04-27
Blue Bird Recalls 2023 Vision School Buses for Stop Arm Defect
Blue Bird is recalling 2023 Vision school buses because incorrect pins on the air stop arm may cause it to fail, increasing injury risk during boarding.
Product
BLUE BIRD — BLUE BIRD VISION SCHOOL BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0978-2022·2022-04-27
Medical device X-ray imaging system recalled for cooling failure
Siemens Medical Solutions is recalling its Artis Q.zen X-ray imaging system due to a coolant circulation defect that may cause insufficient tube cooling and system shutdown.
Product
Artis Q.zen floor, Model Number 10848353
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V281000·2022-04-27
Daimler Recalls 2019-2021 Sprinter Vehicles for Rearview Camera Software Error
Daimler Vans USA is recalling 2019-2021 Freightliner and Mercedes-Benz Sprinter vans because a software error may prevent the rearview camera from displaying an image.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 1500, SPRINTER 4500, SPRINTER 2500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0985-2022·2022-04-27
Medical imaging system software errors may delay treatment procedures
Siemens Artis icono biplane diagnostic imaging systems may experience software errors affecting block movements and detector rotation, potentially delaying treatment until the system is restarted.
Product
Artis icono biplane- in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). Intended use single and biplane diagnostic imaging and interventional procedures. Model: 11327600
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0778-2022·2022-04-27
Injectable Drug Recalled Due to Sterility Assurance Concerns
North American Custom Laboratories is recalling LL-37 2 mg/mL injectable vials due to manufacturing process deviations that raise questions about product sterility. The company distributed 25 vials nationwide.
Product
LL-37 2 mg/mL (5 mL) Injection, 5 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0974-2022·2022-04-27
Artis Q floor X-ray system cooling failure poses overheating risk
Siemens is recalling 80 Artis Q floor X-ray systems nationwide due to a cooling circuit failure that may cause insufficient cooling of the X-ray tube, resulting in automatic system shutdown.
Product
Artis Q floor, Model Number 10848280
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0989-2022·2022-04-27
Gallant VR Implantable Cardioverter Defibrillator Bluetooth malfunction impairs remote monitoring
Certain Gallant VR Implantable Cardioverter Defibrillator units experience Bluetooth malfunction preventing remote monitoring and reducing battery longevity.
Product
Gallant VR Implantable Cardioverter Defibrillator REF # CDVRA500Q
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0969-2022·2022-04-27
Medical X-ray imaging system recalled for cooling circuit malfunction
Siemens' Artis zee X-ray imaging systems may have inadequate cooling if the coolant level drops, potentially causing X-ray tube overheating. The system displays warnings and blocks X-ray operation to prevent equipment damage.
Product
Artis zee multi-purpose, Model Number 10094139
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0987-2022·2022-04-27
Siemens Artis pheno diagnostic imaging system software malfunction recall
Siemens Medical Solutions is recalling 20 Artis pheno diagnostic imaging systems nationwide due to software errors in block movement and detector rotation functions. The malfunction may limit device functionality and delay clinical treatment until the system restarts.
Product
Artis pheno- in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). Intended use-single and biplane diagnostic imaging and interventional procedures. Model: 10849000
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0957-2022·2022-04-27
Abbott TactiCath Ablation Catheters Recalled for Software-Disabled Devices
Abbott has recalled 588 TactiCath ablation catheters that were preprogrammed with a 'First Use Date' disabling device functionality. The catheters were distributed worldwide and throughout the U.S.
Product
Abbott SE TactiCath Sensor Enabled Contact Force Ablation Catheter, Bi-D, Curve DD, Model A-TCSE-DD, Sterile.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0779-2022·2022-04-27
Melanotan II Injectable Recalled for Manufacturing Sterility Defect
Melanotan II injection (35 vials) is being recalled nationwide due to manufacturing deviations that could compromise product sterility. Patients should not use affected lots and should contact their healthcare provider.
Product
Melanotan II 1 mg/mL (10 mL) Injection, 10mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0977-2022·2022-04-27
Artis Q zeego X-ray system recalled for inadequate cooling risk
Siemens is recalling 38 Artis Q zeego X-ray systems nationwide due to a cooling circuit malfunction that may prevent adequate cooling of the X-ray tube, triggering automatic system shutdown.
Product
Artis Q zeego, Model Number 10848283
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0959-2022·2022-04-27
Acumed Cannulated Screws Recalled for Insufficient Axial Pullout Strength
Acumed LLC is recalling Cannulated Screws (4.0mm x 12mm) that may not have sufficient strength to hold bone fragments together, risking fracture or joint damage.
Product
4.0mm x 12mm Cannulated Screw, Short Thread; Part number 3005-40012
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0986-2022·2022-04-27
Diagnostic imaging system software malfunction may interrupt clinical procedures
Siemens is recalling 35 Artis icono floor diagnostic imaging systems due to five potential software errors affecting equipment movements and detector control. The defects may limit functionality during procedures and could delay clinical treatment until the system is restarted.
Product
Artis icono floor in combination with a Siemens Healthineers table or Trumpf/MAQUET table (OEM). Intended use single and biplane diagnostic imaging and interventional procedures. Model: 11327700
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0967-2022·2022-04-27
Artis zee floor X-ray systems recalled for cooling system failure
Siemens is recalling 305 Artis zee floor X-ray imaging systems because the cooling circuit may fail to maintain adequate coolant levels, potentially causing the X-ray tube to overheat. The system includes automatic safeguards that shut down X-ray operation if overheating is detected.
Product
Artis zee floor, Model Number 10094135
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0775-2022·2022-04-27
Injectable Drug Recall: ARA-290 Due to Sterility Manufacturing Defects
ARA-290 (Cibinetide Acetate) injection is recalled due to manufacturing deviations that call sterility into question. Patients should contact their healthcare provider, as 28 vials have been distributed nationwide.
Product
ARA-290 (Cibinetide Acetate) 6 mg/mL (4 mL) Injection, 4 mL vials, Rx only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081 USA
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0780-2022·2022-04-27
PT-141 Injection Recalled for Sterility Assurance Defect
PT-141 (Bremelanotide) injection vials are recalled due to manufacturing deviations that compromise sterility assurance. The FDA Class II recall involves 43 vials distributed nationwide.
Product
PT-141 (Bremelanotide Acetate) 10 mg/mL (2 mL) Injection, 2mL vials, Rx Only, Farmakeio 1736 N Greenville Ave Richardson, TX 75081
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0976-2022·2022-04-27
Artis Q biplane X-ray systems cooling failure may prevent adequate tube cooling
Siemens is recalling 269 Artis Q biplane X-ray systems due to potential coolant level drops that may prevent the X-ray tube from cooling adequately, triggering automatic system shutdown.
Product
Artis Q biplane, Model Number 10848282
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0960-2022·2022-04-27
HUNTLEIGH Disposable Intraoperative Probe recalled for detachable faceplate
Huntleigh Healthcare Ltd. is recalling 150 HUNTLEIGH Disposable Intraoperative Probes (8MHz) because the faceplate may become detached from the probe body during use.
Product
HUNTLEIGH Disposable intraoperative Probe, 8Mhz (box), REF DIPP10, containing 10 individual Disposable Intraoperative Probes, REF DIOP8
Category
Medical Device
Distribution
Distributed nationwide