State

US Virgin Islands product recalls

73,738 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 178
Critical: 12
Severe: 39
Most recent: 2026-10-21

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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38676–38700 of 73916

SevereFDA (Devices)·Z-1608-2018·2018-05-09
Philips MultiDiagnostic-Eleva Recalled Due to Uncontrolled Table Rotation Hazard
Philips Medical Systems is recalling 184 MultiDiagnostic-Eleva systems because a broken actuator fixation can cause the table to rotate uncontrollably at high speed.
Product
MultiDiagnostic-Eleva with Flat Detector 708038 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1604-2018·2018-05-09
Philips URODiagnost Imaging System Recalled Due to Uncontrolled Table Rotation
Philips Medical Systems is recalling 20 URODiagnost imaging systems because the tilt actuator fixation may break, causing the table to rotate uncontrollably at high speed.
Product
708033 URODiagnost As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography can be Performed along with more specialized interventional applications on human patients.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-1476-2018·2018-05-09
FDA Recalls Mitragyna Speciosa Leaf Powder Due to Salmonella Contamination Risk
Viable Solutions, LLC is recalling Mitragyna Speciosa Leaf Powder products because they may be contaminated with Salmonella.
Product
Mitragyna Speciosa Leaf Powder Red Vein Sumatra and Mitragyna Speciosa Leaf Powder Red Vein Bali, sold under the brand name Herbal-Salvation.com. The powder is packaged in kraft paper, foil-lined heat sealed pouches and sold in 25g, 100g, 250g, and 1000g. The product label…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1592-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Exhaust Lines Due to Sterility Concerns
Cook Inc. is recalling 760 StoneBreaker Exhaust Lines because the interior may not be properly sterilized during reprocessing.
Product
StoneBreaker Exhaust Line, Catalog number: SBA-EL; GPN: G52600; UDI: (01)00827002526006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1144-2018·2018-05-09
Purely Elizabeth Granola Recalled for Undeclared Soy Lecithin
Purely Elizabeth is recalling Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin. The product was distributed nationwide.
Product
Chocolate Sea Salt Probiotic Granola, Purely Elizabeth, 8oz, PET/LLDPE Pouch, 6 units/case,
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1540-2018·2018-05-09
Siemens Dimension Vista Calcium Flex Reagent Cartridge Recalled for Low Results
Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium Flex reagent cartridges because they may produce erroneously low results from specific well sets.
Product
Dimension Vista¿ Calcium Flex¿ reagent cartridge, Dimension Vista¿ CA, K1023, SMN # 10445160 The CA method is an in vitro diagnostic test for the quantitative measurement of calcium in human serum, plasma, and urine on the Dimension Vista System.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1595-2018·2018-05-09
Cook Inc. Recalls StoneBreaker C02 Cartridges Due to Sterility Concerns
Cook Inc. is recalling 38,542 StoneBreaker C02 Cartridges because the interior may not be sterilized to the appropriate level when reprocessed.
Product
StoneBreaker C02 Cartridge, Catalog number: SBC-10; GPN: G52603; UDI: (01)10827002526034
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1593-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Probe Caps Due to Sterility Concerns
Cook Inc. is recalling 370 StoneBreaker Probe Caps because the interior may not be properly sterilized during reprocessing.
Product
StoneBreaker Probe Cap, Catalog number:SBA-PC; GPN: G52601; UDI:(01)00827002526013
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1591-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Exhaust Caps Due to Sterility Concerns
Cook Inc. is recalling 629 StoneBreaker Exhaust Caps because the interior may not be sterilized to the appropriate level when following reprocessing instructions.
Product
StoneBreaker Exhaust Cap, Catalog number: SBA-EC; GPN: G52599; UDI: (01)00827002525993
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18740·2018-05-09
Wrapables Recalls Women's Silk Scarves for Flammability Standard Violation
Wrapables is recalling about 1,900 women's silk scarves because they fail to meet federal flammability standards, posing a risk of burn injuries.
Product
Women's scarves
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·18V302000·2018-05-09
Triumph Recalls 2018 Street Triple Motorcycles for Switch Malfunction
Triumph is recalling 2018 Street Triple R and RS motorcycles because water intrusion can cause the turn signal and headlight switches to malfunction, increasing crash risk.
Product
TRIUMPH — TRIUMPH STREET TRIPLE S
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·18151·2018-05-09
Specialized Recalls Bicycles with Stout Cranks Due to Fall Hazards
Specialized is recalling about 1,800 Fuse Comp and Fatboy SE bicycles with Stout cranks because the driveside crankarm can disengage, posing fall and injury hazards.
Product
Specialized bicycles with Stout cranks
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1590-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Pneumatic Lithotripter Due to Sterility Concerns
Cook Inc. is recalling 751 units of the StoneBreaker Pneumatic Lithotripter because the device may not be properly sterilized during reprocessing.
Product
StoneBreaker Pneumatic Lithotripter, Catalog number: SBL-KIT1; GPN: G52604 UDI:(01)00827002526044
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1582-2018·2018-05-09
Radiometer AQURE Software Recalled for Potential Patient Data Mix-Up
Radiometer Medical ApS is recalling AQURE software versions 2.3.0 and 2.3.1 due to a potential problem that may result in patient mix-up.
Product
AQURE, Software version 2.3.0 and 2.3.1 Product Usage: The AQURE system is intended to let allow the management of analytical devices and operator profiles. The user can associate patient data with test data. The system shows test results. The system receives data from…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1596-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Single Use Probes for Sterility Concerns
Cook Inc. is recalling 12,556 StoneBreaker Single Use Probes because the interior may not be properly sterilized. The recall covers units distributed in the US and 70 other countries.
Product
StoneBreaker Single Use Probe, Catalog numbers: SBP-010500; SBP-010605; SBP-016500; SBP-016605; SBP-020425 GPN : G52607; G52605; G52606; G52609; G52608
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1537-2018·2018-05-09
Zimmer Biomet Recalls Modular Hip Head Components Due to Sizing Errors
Zimmer Biomet is recalling 30 modular hip head components because two lots of different sizes were potentially commingled. This error could lead to the use of an incorrect sized head, causing surgery delays or dislocation.
Product
Modular Head Component, Biomet Hip System; Item No. 163669, Hip Joint, metal/polymer semi-constrained cemented prosthesis The device is used in treatment of patients who need total hip arthroplasty, and consists of modular components and corresponding instruments.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1594-2018·2018-05-09
Cook Inc. Recalls StoneBreaker Sterilization Caps Due to Sterility Concerns
Cook Inc. is recalling 470 StoneBreaker Sterilization Caps because the interior may not reach the required Sterility Assurance Level during reprocessing.
Product
StoneBreaker Sterilization Cap, Catalog number: SBA-SC; GPN: G52602; UDI: (01)00827002526020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1597-2018·2018-05-09
Siemens Biograph Horizon PET/CT Scanner Software Recall for Image Errors
Siemens Medical Solutions is recalling 42 Biograph Horizon PET/CT scanners due to a software error that causes incorrect image reconstruction.
Product
Biograph Horizon - PET/CT, PETsyngo VJ20A Software Nuclear medicine/ xray diagnostic scanner.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1613-2018·2018-05-09
Roche cobas b 221 AutoQC Module Recall for Software Failure
Roche Diagnostics is recalling cobas b 221 AutoQC Modules because a software defect prevents the scheduled quality control measurements from starting.
Product
cobas b 221 AutoQC Module Complete; Catalog numbers: 3313522001 and 3313522692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1610-2018·2018-05-09
Roche Omni S2 Analyzer Recall Due to Software Failure
Roche Diagnostics is recalling 1,026 Omni S2 analyzers because a software defect prevents scheduled quality control measurements from starting.
Product
cobas b 221<2>Roche OMNI S2 system catalog numbers: 3337111001 and 3337111692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride, hematocrit…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0710-2018·2018-05-09
Rhodes Pharmaceuticals Recalls Aptensio XR Capsules Due to Dissolution Failure
Rhodes Pharmaceuticals is recalling Aptensio XR capsules because they failed to meet dissolution specifications. The affected lot was distributed nationwide.
Product
Aptensio XR (methylphenidate HCl extended-release) capsules 15 mg Rx Only 90-count bottle. Marketed by: Rhodes Pharmaceuticals L.P., Coventry, RI 02816. Manufactured by: Patheon Manufacturing Services LLC, Greenville, NC 27834. NDC 42858-402-45
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1611-2018·2018-05-09
Roche OMNI S4 Analyzer Recalled for Software Scheduler Failure
Roche Diagnostics is recalling 1,026 OMNI S4 analyzers because a software defect prevents the AutoQC scheduler from activating.
Product
Cobas b 221<4>Roche OMNI S4 system; Catalog numbers: 3337138001 and 3337138692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1584-2018·2018-05-09
CooperSurgical Recalls 5 mm Apple-Hunt Secondary Cannulas Due to Packaging Error
CooperSurgical, Inc. is recalling 520 units of 5 mm Apple-Hunt Secondary Cannulas because they were packaged with the wrong trocar length type.
Product
5 mm Apple-Hunt Secondary Cannula/Pyramidal Tip Trocar - extended length (5 count); Model Number 900-840 Product Usage: The Apple-Hunt Secondary Cannulas are indicated for use in laparoscopic surgical procedures to provide a pathway for the introduction of endoscopic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1612-2018·2018-05-09
Roche OMNI S6 Analyzer Software Defect Recalled by FDA
Roche Diagnostics is recalling 1,026 OMNI S6 analyzers because a software defect prevents scheduled AutoQC measurements from starting.
Product
cobas b 221<6>Roche OMNI S6 system; Catalog numbers: 3337154001 and 3337154692 The Roche Diagnostics Omni S Analyzer is a fully automated critical care analyzer intended to be used for the measurement of pH, PCO2, PO2, sodium, potassium, ionized calcium, chloride…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1615-2018·2018-05-09
IntroMedic Recalls Miriam Capsule Endoscope System Due to Battery Indicator Error
IntroMedic Co., Ltd. is recalling 82 units of the Miriam Capsule Endoscope System because the battery indicator may incorrectly display orange when the battery is fully charged.
Product
Miriam Capsule Endoscope System. Model MR1100 Product Usage: MiroCam Capsule Endoscope System is intended for visualization of the small bowel mucosa. It may be used as a tool in the detection of abnormalities of the small bowel in adults.
Category
Medical Device
Distribution
Distributed nationwide