State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53301–53325 of 74002

HighFDA (Devices)·Z-1965-2015·2015-07-08
Hamilton Medical Infant Flow Sensor Recalled for Inaccurate Ventilation Measurements
Hamilton Medical is recalling Infant Flow Sensors because inaccurate flow measurements may cause ventilators to decrease ventilation delivery.
Product
Hamilton Medical Infant Flow Sensor, single use, (3.1m), Part number 260179. The infant flow sensor is an accessory for the Hamilton Medical Ventilators. Product Usage: The infant flow sensor is a device to measure patient air flow and pressures within the Hamilton Medical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1948-2015·2015-07-08
Zimmer Recalls Natural Knee II Revision Femoral Stems Due to Sterility Breach
Zimmer, Inc. is recalling 352 Natural Knee II Revision Femoral Stems because a breach in the sterile barrier could lead to periprosthetic infection.
Product
Natural Knee II Revision Femoral Stem, 125mm, item 6215-12-185. packaged in configuration 803/791. Knee Prosthesis component.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1854-2015·2015-07-08
Palindrome SI Chronic Catheter Kit Recalled for Antimicrobial Specification Failure
Covidien LLC is recalling Palindrome SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects units distributed worldwide with expiry dates of February 2018 and earlier.
Product
Palindrome SI Chronic Catheter Kit 14.5 Fr x 28cm Item Code: 8888245064
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1932-2015·2015-07-08
Abbott ICT Serum Calibrator Recalled for Inaccurate Potassium Results
Abbott Laboratories is recalling ICT Serum Calibrator REF 146-03 because it may generate lower than expected Potassium results on the Abbott Architect cSystem.
Product
ICT Serum Calibrator REF 146-03. For use in the calibration of the serum Sodium, Potassium, and Chloride assays.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1864-2015·2015-07-08
Palindrome SI Chronic Catheter Kit Recalled for Antimicrobial Specification Failure
Covidien LLC is recalling Palindrome SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888145065
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1908-2015·2015-07-08
Covidien Recalls Chronic Catheters That May Not Meet Antimicrobial Specifications
Covidien LLC is recalling specific lots of Palindrome Precision HSI Chronic Catheters because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome Precision HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888119369P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1922-2015·2015-07-08
Roche Creatinine Plus Reagent Recalled for Potential Drug Interference
Roche Diagnostics is recalling Creatinine Plus reagents because acetaminophen and N-acetylcysteine may cause falsely decreased test results.
Product
Creatinine Plus. Intended for use on Hitachi/MODULAR systems for the quantitative determination of the creatinine concentration in serum, plasma, and urine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1906-2015·2015-07-08
Palindrome HSI Chronic Catheter Recalled for Antimicrobial Specification Failure
Covidien LLC is recalling Palindrome HSI Chronic Catheters because they may not meet antimicrobial specifications. The recall affects units with expiry dates of February 2018 and earlier.
Product
Palindrome HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888128459
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1875-2015·2015-07-08
Palindrome Precision SI Chronic Catheter Kit Recall for Antimicrobial Defects
Covidien LLC is recalling Palindrome Precision SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 33cmItem Code: 8888145065CP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1874-2015·2015-07-08
FDA Recalls Palindrome Precision SI Chronic Catheter Kits for Antimicrobial Defects
The FDA is recalling Palindrome Precision SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects units with expiry dates of February 2018 and earlier.
Product
Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888145065P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1977-2015·2015-07-08
GE Healthcare Recalls Innova 2121IQ Angiographic X-ray Systems
GE Healthcare is recalling Innova 2121IQ angiographic X-ray systems due to a potential loss of C-arm gantry motion capability.
Product
GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1978-2015·2015-07-08
GE Healthcare Recalls Innova 3100IQ Angiographic X-ray Systems
GE Healthcare is recalling six Innova 3100IQ angiographic X-ray systems due to a potential loss of C-arm gantry motion capability.
Product
GE Healthcare Innova 3100IQ. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1981-2015·2015-07-08
GE Healthcare Recalls Innova IGS 530 Angiographic X-ray Systems
GE Healthcare is recalling 17 Innova IGS 530 angiographic X-ray systems due to a potential loss of C-arm gantry motion capability.
Product
GE Healthcare Innova IGS 530. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1975-2015·2015-07-08
GE Healthcare Recalls Angiographic X-ray Systems Due to Motion Loss
GE Healthcare is recalling three Discovery and Innova IGS 740 angiographic X-ray systems because they may lose C-arm gantry motion capability.
Product
GE Healthcare Discovery IGS 740 & GE Healthcare Innova IGS 740. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1886-2015·2015-07-08
Covidien Recalls Palindrome Precision SI Chronic Catheters for Antimicrobial Issues
Covidien LLC is recalling Palindrome Precision SI Chronic Catheters because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome Precision SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888128458P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1893-2015·2015-07-08
Palindrome HSI Chronic Catheter Kit Recalled for Antimicrobial Specification Failure
The FDA is recalling Palindrome HSI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome HSI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code:8888145049C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1966-2015·2015-07-08
GE Healthcare Radiographic Systems Recalled for Safety Mechanism Failure
GE Healthcare is recalling Precision 500D and Advantx Legacy systems because a safety mechanism may fail to engage, posing a risk of injury from falling equipment.
Product
GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems. A universal diagnostic imaging system for radiographic and fluoroscopic examinations. Applications can be performed with the patient sitting, standing, or lying in the prone or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1976-2015·2015-07-08
GE Healthcare Recalls Innova 2100IQ Angiographic X-ray Systems
GE Healthcare is recalling 13 Innova 2100IQ angiographic X-ray systems due to a potential safety issue that may cause the loss of C-arm gantry motion capability.
Product
GE Healthcare Innova 2100IQ. Angiographic X-ray systems used in generating fluoroscopic and rotational images of human anatomy for diagnostic, interventional and image-guided surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1883-2015·2015-07-08
Palindrome SI Chronic Catheter Recall for Antimicrobial Specification Failure
Covidien LLC is recalling Palindrome SI Chronic Catheters because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888128458
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1962-2015·2015-07-08
Siemens Rapidlab 1265 Blood Gas Analyzer Recalled for Diagnostic Error Code Failure
Siemens Healthcare Diagnostics is recalling 2,713 Rapidlab 1265 blood gas analyzers because specific diagnostic error codes are not functional.
Product
The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1884-2015·2015-07-08
Recall of Palindrome Precision SI Chronic Catheters Due to Antimicrobial Specification Failure
Covidien LLC is recalling Palindrome Precision SI Chronic Catheters because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome Precision SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888119368P
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1861-2015·2015-07-08
FDA Recalls Palindrome SI Chronic Catheter Kits for Antimicrobial Specification Failure
The FDA is recalling Palindrome SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects units with expiry dates of February 2018 and earlier.
Product
Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 23cm Item Code: 8888145063C
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1879-2015·2015-07-08
FDA Recalls Palindrome Precision SI Chronic Catheter Kits for Antimicrobial Failure
The FDA is recalling Palindrome Precision SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome Precision SI Chronic Catheter Kit 14.5 Fr x 55cm Item Code: 8888145066CP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1923-2015·2015-07-08
Roche Creatinine Plus Reagent Recalled for Potential Drug Interference
Roche Diagnostics is recalling Creatinine Plus reagent because it may produce falsely decreased results when used with certain drugs.
Product
Creatinine Plus ver. 2. Intended for use on COBAS INTEGRA systems , cobas c111, and cobas c systems for the quantitative determination of the creatinine concentration in serum, plasma, and urine.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1863-2015·2015-07-08
FDA Recalls Palindrome SI Chronic Catheter Kits for Antimicrobial Specification Failure
The FDA is recalling Palindrome SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects units with expiry dates of February 2018 and earlier.
Product
Palindrome SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888145064C
Category
Medical Device
Distribution
Distributed nationwide