State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59126–59150 of 74011

CriticalFDA (Drugs)·D-1149-2014·2014-03-12
B-50 Capsules Recalled for Containing Unapproved Steroid Ingredients
Mira Health Products Ltd. is recalling B-50 capsules because they contain unapproved steroid ingredients, making them unapproved new drugs.
Product
B-50 capsules, Healthy Life Chemistry By Purity First, packaged in 100 count bottles, Manufactured for: Purity First Health Products, Inc. dba Healthy Life Chemistry 51 Florida Street, Farmingdale, NY 11735
Category
Drug
Distribution
Distributed nationwide
CriticalFDA (Drugs)·D-1150-2014·2014-03-12
Mira Health Recalls Super-DMZ Rx 2.0 Capsules for Unapproved Steroid Ingredient
Mira Health Products Ltd. is recalling Super-DMZ Rx 2.0 Capsules because the product contains an unapproved steroid ingredient and was marketed without FDA approval.
Product
Super-DMZ Rx 2.0 Capsules, 60 count bottles, Dietary Supplement, Lean muscle mass, hardness and strength, Manufactured for Blackstone Labs Boca Raton, FL 33433.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1151-2014·2014-03-12
Mira Health Recalls Unapproved Metha-Drol Extreme Dietary Supplement
Mira Health Products Ltd. is recalling 5,555 bottles of Metha-Drol Extreme capsules because the product contains an unapproved steroid ingredient.
Product
METHA-DROL Extreme capsules, packaged as 60 capsules per bottle Pro-Anabolic Mass Stack Dietary Supplement, Manufactured for Blackstone Labs, Boca Raton, FL
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1096-2014·2014-03-12
Hospira Recalls 0.9% Sodium Chloride Injection Bags Due to Sterility Concerns
Hospira is recalling 603,768 bags of 0.9% Sodium Chloride Injection because solution leaked through the port cover, compromising sterility.
Product
0.9% Sodium Chloride Injection, USP 1000 mL Flexible Container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7983-09
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1143-2014·2014-03-12
Phillips Respironics Recalls Trilogy Ventilators Due to Power Board Defect
Phillips Respironics is recalling 572 Trilogy ventilators worldwide because a defective power management board component may cause loss of therapy.
Product
Trilogy Ventilators The Respironics Trilogy 100 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation. Trilogy 100 is intended for pediatric through adult patients weighing at least 5 kg (11 lbs.). The…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1060-2014·2014-03-12
McKesson Anesthesia Care System Recalled for Data Mismatch
McKesson Technologies is recalling 10 units of the Anesthesia Care system because patient case data did not match the patient data, including data from another case.
Product
McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system is a computer based system which collects, processes,and records data both through manual entry and from monitors which themselves are attached to patients, such as in the operating room environment.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-1148-2014·2014-03-12
Fresenius Kabi Recalls Heparin Sodium Injection Due to Subpotency
Fresenius Kabi is recalling Heparin Sodium Injection vials because they may contain less active ingredient than labeled.
Product
HEPARIN SODIUM — HEPARIN SODIUM (HEPARIN SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1150-2014·2014-03-12
Shimadzu Recalls Mobile X-ray Systems Due to Metal Plate Cracking Risk
Shimadzu Medical Systems is recalling 56 mobile X-ray systems because a connecting metal plate may crack, posing a structural safety risk.
Product
Mobile X-ray System, Model: MUX-100, MUX-100H Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannnot move and/or of outpatients in emergency
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·14V120000·2014-03-12
Keystone Recalls 2014 Fifth Wheels and Travel Trailers for Axle Bearing Defect
Keystone is recalling specific 2014 fifth wheels and travel trailers because insufficient lubrication in the inner wheel bearings may cause the wheel to seize or separate, increasing crash risk.
Product
KEYSTONE — KEYSTONE BULLET, SPRINGDALE, PASSPORT, HIDEOUT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V119000·2014-03-12
Zero Motorcycles Recalls 2014 Models Due to Motor Rotor Contact
Zero Motorcycles is recalling specific 2014 FX, S, DS, and SR models because the motor rotor may contact the stator, potentially causing the rear wheel to lock up and increasing crash risk.
Product
ZERO — ZERO S, DS, SR, FX
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1082-2014·2014-03-12
Elekta Desktop Pro Linear Accelerator Control Software Recalled for Calibration Errors
Elekta, Inc. is recalling Desktop Pro linear accelerator control software because incorrect values may be entered during calibration procedures.
Product
Desktop Pro TM linear accelerator control software intended to assist a licensed practitioner in the delivery of radiation to defined target volumes.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1147-2014·2014-03-12
Hospira Recalls Bupivacaine Hydrochloride Vials Due to Particulate Matter
Hospira Inc. is recalling 115,500 vials of Bupivacaine Hydrochloride injection due to a confirmed report of visible particulate matter embedded in the glass vials.
Product
BUPIVACAINE HYDROCHLORIDE — BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighCPSC·14129·2014-03-12
Fitbit Recalls Force Activity-Tracking Wristband Due to Skin Irritation Risk
Fitbit is recalling Force activity-tracking wristbands because the materials can cause skin irritation, rashes, or blistering. Consumers should contact Fitbit for a full refund.
Product
Wireless activity-tracking wristband
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1084-2014·2014-03-12
Elekta Agility Software Recall for Calibration Input Errors
Elekta is recalling Agility software version 3.0 because incorrect values can be entered during calibration procedures for medical linear accelerators.
Product
Agility. Version 3.0 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators which is associated with Agility collimators.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1085-2014·2014-03-12
Elekta Agility software recall for potential calibration input errors
Elekta is recalling Agility software version 3.1 for linear accelerators because incorrect values could be entered during calibration procedures.
Product
Agility. Version 3.1 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators which is associated with Agility collimators.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V115000·2014-03-12
Triple E Recalls 2014 Free Spirit Motorhomes Due to Obstructed Taillight
Triple E Recreational Vehicles is recalling 2014 Free Spirit motorhomes because the spare tire carrier obstructs the driver's side taillight, increasing crash risk.
Product
FREE SPIRIT — FREE SPIRIT FS22, FS22TE, FS22SS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1083-2014·2014-03-12
Elekta Integrity Software Recalled for Calibration Input Errors
Elekta, Inc. is recalling Integrity Version 1.1 software for linear accelerators because incorrect values can be entered during calibration procedures.
Product
Integrity. Version 1.1 of the Integrity interface and control software for the Elekta range of medical digital linear accelerators.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1147-2014·2014-03-12
GE Healthcare Recalls Solar 8000M/i Patient Monitors Due to AVOA Feature Failure
GE Healthcare is recalling Solar 8000M and 8000i patient monitors because the Automatic-View-On-Alarm feature may stop functioning after a specific discharge event.
Product
GE Healthcare Solar 8000M and Solar 8000i Patient Monitor software version 5.4, 5.5, or 5.6 with the Automatic-View-On- Alarm (AVOA) feature enabled. The Solar 8000i with Patient Data Module / Transport Pro with Patient Data Module is intended for use under the direct…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1128-2014·2014-03-12
Carestream Recalls Kodak 2200 Intraoral X-Ray Systems Due to Arm Failure
Carestream Health is recalling Kodak 2200 Intraoral X-Ray Systems because the device arms may break early. This affects 347 units distributed in the US and Canada.
Product
Model Kodak 2200 Intraoral X-Ray System, Catalog Numbers 5303177, 5303169, 5303151, XR-5154323 -- Carestream Health, Inc. Made in France -- --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray, Extraoral with timer --- There are four major…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1124-2014·2014-03-12
Medical Information Technology Recalls MEDITECH Microbiology Calculator Module
Medical Information Technology, Inc. is recalling MEDITECH Microbiology calculator modules due to a risk of patient results being removed from laboratory and electronic medical record systems.
Product
MEDITECH Microbiology - Calculator/data processing module, for clinical use.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1127-2014·2014-03-12
Carestream Recalls Kodak 2100 Intraoral X-Ray Systems Due to Arm Breakage
Carestream Health is recalling Kodak 2100 Intraoral X-Ray Systems because the device arms may break early. The recall covers 347 units distributed in the US and Canada.
Product
Model Kodak 2100 Intraoral X-Ray System, Catalog Numbers 5303144, 8011579 -- Carestream Health, Inc. 150 Verona Street Rochester, NY 14608 -- Made in France -- TROPHY 77435 Marne La Vallee --- COMMON/USUAL NAME: Dental X-Ray Systems -- CLASSIFICATION NAME: Unit, X-Ray…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1141-2014·2014-03-12
KCI Recalls Prevena Incision Management System Due to Connector Difficulty
KCI USA is recalling 20,850 units of the Prevena Incision Management System because the tubing connector is difficult to attach to the canister.
Product
PRE2001US: Prevena Incision Management Customizable System Box (US-ONLY) Product Usage: The Prevena Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1091-2014·2014-03-12
Actavis Recalls Alprazolam Extended-Release Tablets for Dissolution Failures
Actavis Elizabeth LLC is recalling 5,148 bottles of Alprazolam Extended-Release Tablets, 3 mg, because the product failed to meet dissolution specifications.
Product
Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-3086-06, UPC 3 0228-3086-06 2.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1095-2014·2014-03-12
Teva Recalls Hydroxyzine Pamoate Capsules Due to Unapproved Manufacturing Material
Teva Pharmaceuticals is recalling specific lots of Hydroxyzine Pamoate capsules because they were manufactured using an unapproved active pharmaceutical ingredient.
Product
HYDROXYZINE PAMOATE — HYDROXYZINE PAMOATE (HYDROXYZINE PAMOATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1131-2014·2014-03-12
AlterG Anti-Gravity Treadmill Accessory Shorts Recalled for Unapproved Material
AlterG, Incorporated is recalling 2,221 accessory shorts for the AlterG Anti-Gravity Treadmill because unapproved material caused them to stretch unusually, making them uncomfortable for patients.
Product
Accessory shorts for the AlterG Anti-Gravity treadmill. Use with the AlterG Anti-Gravity Treadmill for rehabilitation.
Category
Medical Device
Distribution
Distributed nationwide