State

US Virgin Islands product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

46476–46500 of 73987

SevereFDA (Devices)·Z-2880-2016·2016-10-05
Trividia Health Recalls TRUEread Blood Glucose Test Strips for Incorrect Readings
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels, potentially affecting patient safety.
Product
TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-2784-2016·2016-10-05
Anspach Effort Recalls Small Battery Drive Adaptors Due to Burst Risk
The Anspach Effort, Inc. is recalling 1,833 Small Battery Drive adaptors worldwide because they may generate excessive internal pressure and burst.
Product
Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive (SBD) /Small Battery Drive II (SBD II) is designed for use in traumatology and orthopedic surgery of the skeleton, i.e. drilling, reaming or cutting bone. The…
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·16V712000·2016-10-05
Daimler Recalls 2017 Thomas Built Buses Saf-T-Liner C2 School Bus Chassis
Daimler Trucks North America is recalling 162 model year 2017 Thomas Built Buses Saf-T-Liner C2 school bus chassis because the brake transmission shift interlock may be inoperable.
Product
THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V709000·2016-10-05
NHTSA Recalls 2015-2016 Wells Cargo and Haulmark Snowmobile Trailers
Universal Trailer Cargo Group is recalling 89 aluminum snowmobile trailers because cross winds may cause them to tip or lift, potentially tearing the couplers.
Product
WELLS CARGO — WELLS CARGO, HAULMARK ALUMINUM SNOWMOBILE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2896-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 47,989 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients.
Product
Zyno Medical Administration Set Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: B2-70072-F Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a container to a patients vascular system through a needle…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2882-2016·2016-10-05
Trividia Health Recalls TRUEread Blood Glucose Test Strips for Inaccurate Readings
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels. The recall affects strips and kits distributed in the US and internationally.
Product
TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2886-2016·2016-10-05
Spacelabs Xhibit Telemetry Receiver Recall for System Lockups
Spacelabs Healthcare is recalling Xhibit Telemetry Receivers because the system may go offline or lock up, potentially failing to display alarms.
Product
Spacelabs Healthcare Xhibit Telemetry Receiver (XTR), Model 96280. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient vital signs.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2877-2016·2016-10-05
Siemens PRIMUS Linear Accelerators Recalled for Software Safety Issues
Siemens Medical Solutions is recalling 103 PRIMUS linear accelerators to install a software patch addressing several safety issues.
Product
PRIMUS, Accelerator, Linear, Medical The PRIMUSTM family of linear accelerator systems is to deliver x-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2895-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 78,063 sterile administration sets due to a potential filter leaking defect. The sets are distributed nationwide for use with infusion pumps or gravity feed.
Product
Zyno Medical Administration Set, Sterile. RX For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: B2-70071-DF Product Code: B2-70071-DF-120 (expanded recall) Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2888-2016·2016-10-05
Spiegelberg Brain Pressure Monitoring Probes Recalled for Measurement Errors
Spiegelberg is recalling 22 Brain Pressure Monitoring System probes due to air chamber shrinkage that caused false high readings in the lower measuring range.
Product
Spiegelberg Brain Pressure Monitoring System Probe 3PN, REF: SNDI3.1.531FV534P and Probe 3PS, REF: SNDI3.1.63/FV535P Product Usage: lntracranial pressure measuring probes are used to measure intracranial pressure (intracranial pressure, ICP), so the pressure in the head.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2881-2016·2016-10-05
Trividia Health Recalls TRUEread Blood Glucose Test Strips for Inaccurate Readings
Trividia Health is recalling TRUEread Blood Glucose Test Strips because they may provide incorrect low blood glucose levels.
Product
TRUEread Blood Glucose Test Strips (Glucose Oxidase) are used with TRUEresult and TRUE2go meters. TRUEread Blood Glucose Test Strips are available in vials with 10 ct., 25 ct., 50 ct., and sold as 10 ct. with meters. Quantitatively measure whole blood glucose in a…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V710000·2016-10-05
Altec Recalls 2014-2015 Aerial Devices Due to Boom Tip Cover Defect
Altec is recalling 219 model year 2014-2015 aerial devices because an improperly sized boom tip cover opening may allow contact with energized conductors, increasing injury risk.
Product
ALTEC — ALTEC AERIAL DEVICE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2893-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 114,081 sterile administration sets due to a potential filter leaking defect. The sets are used to administer fluids to patients' vascular systems.
Product
Zyno Medical Administration Set, Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: A2-80071-DF Product Code: A2-80071-DF-120 (Expanded recall) Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2885-2016·2016-10-05
Spacelabs Xhibit Central Station Recalled for System Lockups and Alarm Failures
Spacelabs Healthcare is recalling Xhibit Central Stations because the telemetry system may go offline, lock up, or fail to display audio and visual alarms for asystole.
Product
Spacelabs Healthcare Xhibit Central Station, Model 96102, Version 1.1.2. Xhibit Telemetry Receivers (XTR) must be connected to an Xhibit Central Station for the display of patient vital signs.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·16V711000·2016-10-05
Western Star Trucks Recall for Seat Belt Mounting Plate Defect
Daimler Trucks North America is recalling 2014-2017 Western Star 4900 and 5700 trucks because a seat belt mounting plate may have a hole that is too large, increasing injury risk in a crash.
Product
WESTERN STAR — WESTERN STAR 5700, 4900
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2894-2016·2016-10-05
Zyno Medical Administration Set Recalled for Potential Filter Leaking
Zyno Medical LLC is recalling 78,069 sterile administration sets because the filter may leak. The sets are used to administer fluids to patients.
Product
Zyno Medical Administration Set, Sterile. Rx For Use with Zyno Medical Infusion Pumps or Gravity Feed Product Code: A2-80072-F Product Usage: Zyno Medical Administration Set is a device used to administer fluids from a container to a patients vascular system through a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2878-2016·2016-10-05
Siemens Syngo RT Therapist Software Recalled for Safety Issues
Siemens Medical Solutions is recalling Syngo RT Therapist software to address several safety issues. The recall affects 103 linear accelerators nationwide.
Product
Syngo RT Therapist, Accelerator, Linear, Medical Syngo RT Therapist is a software application whose indication for use includes the viewing, processing, filming, and archiving of medical images. It also permits patient data management, patient selection/setup, patient…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2876-2016·2016-10-05
Siemens ARTISTE Linear Accelerators Recalled for Software Safety Issues
Siemens Medical Solutions is recalling 103 ARTISTE linear accelerators to install a software patch addressing several safety issues.
Product
ARTISTE, Accelerator, Linear, Medical The intended use of the SIEMENS branded ARTISTETM family of linear accelerator systems is to deliver X-Ray photon and electron radiation for the therapeutic treatment of cancer.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2879-2016·2016-10-05
CareFusion Recalls Alaris Syringe Modules Due to Software Anomaly
CareFusion 303, Inc. is recalling Alaris Syringe Module Model 8110 units with software version 9.15 because a software anomaly may cause infusions to stop unexpectedly.
Product
Alaris Syringe Module Model 8110 with software version 9.15 The Alaris Syringe Pump module is part of the Alaris System. The syringe pump delivers fluids in a manner similar to current syringe pumps on the market. Up to four Alaris Syringe pump modules can be connected to the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2892-2016·2016-10-05
Siemens Medical Solutions Recalls Syngo.plaza VB10A Picture Archiving Systems
Siemens Medical Solutions USA, Inc. is recalling 47 Syngo.plaza VB10A Picture Archiving and Communication Systems to eliminate several software issues.
Product
Syngo.plaza VB10A, Picture Archiving and Communication System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2891-2016·2016-10-05
Siemens Syngo.plaza PACS Software Recall for Multiple Issues
Siemens Medical Solutions is recalling 47 Syngo.plaza Picture Archiving and Communication System units to address several software issues.
Product
Syngo.plaza, Picture Archiving and Communication System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-2602-2016·2016-10-05
Goya Honey with Comb Recalled for Unregistered Chemical Presence
Tradewind Foods is recalling Goya Honey with Comb because FDA testing found 2,6-Dichlorobenzamide, a chemical not registered for use in honey.
Product
Label reads in part as " GOYA ***HONEY WITH COMB***PURE ALL NATURAL***NET WT. 16 OZ (1LB)***15173***GOYA FOODS, INC. SECAUCUS, NJ 07096"
Category
Food
Distribution
2 states
ModerateFDA (Drugs)·D-1525-2016·2016-10-05
Pharmatech Recalls Senexon Liquid Due to Potential B. cepacia Contamination
Pharmatech LLC is recalling Senexon Liquid (sennosides) 8.8 mg bottles nationwide as a precautionary measure due to a potential risk of contamination with B. cepacia bacteria.
Product
Senexon Liquid (sennosides) 8.8 mg, 8 fl oz. (237 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1000-59.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2884-2016·2016-10-05
Microgenics Recalls DRI Salicylate Serum Tox Assay Due to Sensitivity Issues
Microgenics Corporation is recalling specific lots of DRI Salicylate Serum Tox Assay kits because negative patient samples are recovering higher than the product's sensitivity claim.
Product
DRI Salicylate Serum Tox Assay, Catalog number 0977. Toxicology: The DRI Salicylate Serum Tox Assay is intended for the quantitative determination of salicylate in human serum or plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1523-2016·2016-10-05
Pharmatech Recalls Aller-Chlor Syrup Due to Potential B. cepacia Contamination
Pharmatech LLC is recalling 12,308 bottles of Aller-Chlor Syrup nationwide due to a potential risk of contamination with B. cepacia bacteria.
Product
Aller-Chlor (chlorpheniramine maleate) Syrup, USP, 2 mg in each 5 mL, 4 fl oz (120 mL) bottle, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, NDC 0536-1025-47.
Category
Drug
Distribution
Distributed nationwide