State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56901–56925 of 74005

SevereFDA (Devices)·Z-2619-2014·2014-10-01
ICU Medical Recalls STAT 2 Flow Controllers Due to High Flow Rate
ICU Medical is recalling STAT 2 Flow Controllers because they may deliver a significantly higher flow rate than intended.
Product
STAT 2 Flow Controller; 80" (203 cm) Appx 14.8 mL, 20 Drop Primary Set w/2 Clave, STAT 2 Flow Controller, Rotating Luer, Item No. 011-C9801. Product Usage: IV Administration sets are intended for the infusion and withdrawal of fluids. The devices are provided sterile.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2707-2014·2014-10-01
Spacelabs Patient Monitor Recall for Missing Audible Alarms in End Case Mode
Spacelabs Healthcare is recalling 222 patient monitors because they may fail to provide audible alarms in End Case mode, a defect missed in a previous recall.
Product
Spacelabs Medical Patient Monitor is a Physiological, Patient monitor With Arrhythmia Detection or Alarms. The Models are 91367, 91369, 91370, 91387, and 91393 are sold with Perioperative Mode (option D), which includes Start case/End case functionality, Upgrade Kit 040-1548-00.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1606-2014·2014-10-01
Baxter Recalls Potassium Chloride Bags Due to Mispackaging Error
Baxter Healthcare is recalling 148,632 bags of Potassium Chloride Injection because shipping cartons were incorrectly labeled and contained Gentamicin Sulfate Injection instead.
Product
POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2698-2014·2014-10-01
Argon UltraStream Hemodialysis Catheter Recalled for Luer Cracking
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during attachment or manipulation.
Product
UltraStream Peel Away Kit; Model Numbers 32401524 (24 cm), 32401528 (28cm), 32401532 (32 cm), and 32401536 (36 cm) and 32402540 (40 cm) The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2675-2014·2014-10-01
Peters Surgical Recalls CARDIOXYL Sutures Due to Surface Treatment Splitting
Peters Surgical is recalling 4,976 units of CARDIOXYL synthetic surgical sutures because a potential splitting of the surface treatment on thread ends was identified.
Product
The synthetic non-absorbable surgical sutures CARDIOXYL are composed of a polyester [poly(ethylene terephtalate)] braids, with or without PLEDGET of different sizes. CARDIOXYL braids are coated with polysiloxane. CARDIOXYL sutures are green dyed (D&C green # 6, CI 61565) and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2703-2014·2014-10-01
Vapotherm Precision Flow Disposable Patient Circuit Recalled for Water Leakage
Vapotherm is recalling 22,042 Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
Product
Vapotherm Precision Flow,Disposable Patient Circuit PF-DPC-Low. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2689-2014·2014-10-01
CareFusion AirLife Heated Infant Breathing Circuit Recalled for Material Change
CareFusion is recalling approximately 318,280 heated infant breathing circuits due to a regulatory compliance risk involving a material change to the gas pathway.
Product
CareFusion AirLife Heated Infant Breathing Circuit Product Usage: Respiratory breathing circuits are used with a ventilator when mechanical ventilation is administered to a patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2700-2014·2014-10-01
Vapotherm Precision Flow Disposable Patient Circuit Recalled for Water Leakage
Vapotherm, Inc. is recalling 1,005 units of Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
Product
Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-High. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2569-2014·2014-10-01
Siemens Artis zee and zeego X-ray Systems Recalled for Radiation Release Issue
Siemens is recalling 206 Artis zee and Artis zeego X-ray systems because radiation release can become blocked unnecessarily under certain circumstances.
Product
Artis zee and Artis zeego systems. x-ray, angiographic system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2677-2014·2014-10-01
Genesys Spine Recalls Circular Lock Screws Due to Material Error
Genesys Orthopedics Systems is recalling 642 Circular Lock Screws from the TiLock Pedicle Screw System because a portion of the lot was manufactured with stainless steel instead of the specified titanium alloy.
Product
Circular Lock Screws, part # G826, lot # 11406. The Lock Screws are part of the Genesys Spine TiLock Pedicle Screw System. The TiLock Pedicle Screw System is intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2694-2014·2014-10-01
Alcon Recalls Eye-Pak 7407 Tray Support Covers Due to Seal Issues
Alcon Research, Ltd. is recalling 2,462 Eye-Pak 7407 Tray Support Covers because insufficiently sealed peel pouches may compromise sterility.
Product
eye-pak 7407 Tray Support Cover REF 8065740745
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V612000·2014-10-01
Coach and Equipment Recalls Transit Buses with Cracking Wheelchair Lifts
Coach and Equipment is recalling 2006-2014 transit buses equipped with certain Ricon wheelchair lifts because the platform side plates may crack, posing an injury risk.
Product
COACH AND EQUIPMENT — COACH AND EQUIPMENT CONDOR LT, PHOENIX, ALLEY CAT, PEGASUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2693-2014·2014-10-01
ArjoHuntleigh Recalls Minstrel Mobile Passive Hoists Due to Bolt Failure
ArjoHuntleigh is recalling 18 Minstrel mobile passive hoists because a bolt under the scale may unscrew, posing a risk of the spreader bar detaching during use.
Product
Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended for lifting and transporting adult residents on horizontal floors in hospitals, nursing homes or other health care facilitates. The Minstrel device aids in the lifting, transfer and lowering to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2705-2014·2014-10-01
Vapotherm Precision Flow Disposable Patient Circuit Recalled for Water Leakage
Vapotherm, Inc. is recalling 865 units of Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
Product
Vapotherm Precision Flow,Disposable Patient Circuit PFHDPC-Low. For use with the Heliox Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V613000·2014-10-01
Honda Recalls 2015 Acura TLX AWD for Incorrect Weight Rating Labels
Honda is recalling 2015 Acura TLX AWD vehicles because incorrect weight ratings on the safety label may lead to tire failure if loaded to specifications.
Product
ACURA — ACURA TLX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2697-2014·2014-10-01
Argon UltraStream Hemodialysis Catheter Recall Due to Luer Cracking
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because the red arterial luer may crack during attachment or manipulation.
Product
UltraStream Exchange Kit Model Numbers 32001524 (24 cm), 32001528 (28cm), 32001532 (32 cm), and 32001536 (36 cm) and 32002540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high flow rates at low arterial…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2704-2014·2014-10-01
Vapotherm Precision Flow Disposable Patient Circuit Recall for Water Leakage
Vapotherm, Inc. is recalling 360 units of Precision Flow Disposable Patient Circuits because they allow water to leak into the center gas lumen.
Product
Vapotherm Precision Flow,Disposable Patient Circuit PF-E-DPC-Low. PF-DPC-Low packaged with compatible cannulas for evaluation of the Precision Flow system
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2701-2014·2014-10-01
Vapotherm Precision Flow Disposable Patient Circuit Recalled for Water Leakage
Vapotherm, Inc. is recalling 635 units of Precision Flow Disposable Patient Circuits because they may allow water to leak into the center gas lumen.
Product
Vapotherm Precision Flow,Disposable Patient Circuit PFH-DPC-High. For use with the Heliox Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2676-2014·2014-10-01
Peters Surgical Recalls CARDIOFLON Evolution Sutures for Surface Splitting
Peters Surgical is recalling 22,190 units of CARDIOFLON Evolution sutures due to a potential splitting of the surface treatment on thread ends.
Product
The synthetic non-absorbable surgical sutures CARDIOFLON Evolution are composed of polyester [poly(ethylene terephtalate)] braids, coated, with or without PLEDGETS of different sizes. CARDIOFLON Evolution sutures are green dyed (D&C green # 6, CI 61565) and white (undyed). Some…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2587-2014·2014-10-01
Siemens AXIOM Artis and Artis zee Systems Recalled for X-Ray Release Issue
Siemens is recalling AXIOM Artis and Artis zee angiography systems because a hand switch defect may cause uncontrolled x-ray release.
Product
AXIOM Artis or Artis zee system Product Usage: Axiom Artis and Artis zee / zeego are dedicated angiography systems developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2696-2014·2014-10-01
Argon UltraStream Hemodialysis Catheters Recalled for Luer Cracking Risk
Argon Medical Devices is recalling UltraStream Chronic Hemodialysis Catheters because cracks may develop on the red arterial luer during use.
Product
UltraStream Chronic Hemodialysis Catheter Standard Kit; Model Number 32101524 (24 cm), 32101528 (28cm), 32101532 (32 cm), and 32101536 (36 cm) and 32102540 (40 cm). The Rex Medical UltraStream Chronic Hemodialysis Catheter is a chronic hemodialysis catheter that can achieve high…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2699-2014·2014-10-01
Vapotherm Precision Flow Patient Circuits Recalled for Water Leakage
Vapotherm, Inc. is recalling 22,828 Precision Flow Disposable Patient Circuits because they may allow water to leak into the gas lumen.
Product
Vapotherm Precision Flow, Disposable Patient Circuit PF-DPC-High. For use with the Precision Flow system Precision Flow" is intended for use to add warm moisture to breathing gases from an external source for administration to a neonate/infant, pediatric and adult patients…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2706-2014·2014-10-01
Vapotherm Precision Flow Patient Circuit Recalled for Potential Water Leakage
Vapotherm, Inc. is recalling 207 units of Precision Flow Disposable Patient Circuits because water may leak into the center gas lumen.
Product
Vapotherm Precision Flow,Disposable Patient Circuit PF-NODPC-Low. For use with the Precision Flow system and Ikaria INOmax DSIR ¿ System. This DPC allows clinicians to administer nitric oxide non-invasively via high flow nasal cannula. In the Precision Flow High Flow…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1571-2014·2014-10-01
Akorn Recalls Rifampin for Injection Due to Impurity Specification Failure
Akorn, Inc. is recalling 5,539 vials of Rifampin for Injection USP, 600 mg, because a stability test showed an impurity level exceeding specifications.
Product
Rifampin for Injection USP, 600 mg*/vial (Sterile), supplied in sterile glass vials, Rx only For IV Infusion only, individually boxed, Mfd. for: Akorn, Inc., Lake Forest, IL --- NDC 17478-151-42
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1609-2014·2014-10-01
Apotex Recalls Olanzapine Tablets Due to Subpotent Drug Levels
Apotex Corp. is recalling Olanzapine Orally Disintegrating Tablets 5 mg because testing showed the drug levels were below specification.
Product
Olanzapine Orally Disintegrating Tablets 5 mg, 30-count Bottle, Rx only, Manufactured by Apotex Inc. Toronto, Ontario Canada M9L1T9, Manufactured for Apotex Corp., Weston, Florida 33326, NDC # 60505-3275-03
Category
Drug
Distribution
Distributed nationwide