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.

59251–59275 of 74011

HighFDA (Devices)·Z-1118-2014·2014-03-05
Philips HeartStart MRx Monitor/Defibrillator Recalled for ECG Cable Wear
Philips is recalling HeartStart MRx Monitor/Defibrillators because the ECG trunk cable and connector block may wear prematurely, causing an interrupted ECG signal.
Product
Philips HeartStart MRx Monitor/Defibrillator; Models: M3535A, M3536A, M3536J, M3536M, M3536M5, and M3536MC. Used for the termination of ventricular tachycardia and ventricular fibrillation.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1562-2014·2014-03-05
Newman's Own Salsa Con Queso Recalled for Undeclared Wheat
Newman's Own is recalling Salsa Con Queso, Medium All Natural, 16 oz. jars nationwide due to undeclared wheat.
Product
Newman's Own Salsa Con Queso, Medium All Natural Net Wt.16 oz., packaged in a glass jar UPC 0 20662 00353 9
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1114-2014·2014-03-05
Winco Premier Care Recliner 5570 Recalled for Lock Bar Defect
Winco Mfg. is recalling 369 Premier Care Recliner 5570 units due to a manufacturing defect that may cause the lock bar to fail.
Product
PREMIER CARE RECLINER 5570 with Urethane armrests, Multiple side-table options, 3 position lock-bar, Fully upholstered, OPTIONAL Heat or Heat & Massage, OPTIONAL LiquiCell. The products are a multi position recliners with a steel frame used primarily in long term care or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1120-2014·2014-03-05
Philips HeartStart MRx Defibrillator Batteries Recalled for Shutdown Risk
Philips is recalling 43,792 HeartStart MRx defibrillator batteries because they may shut down unexpectedly when exposed to high electromagnetic interference.
Product
HeartStart MRx Defibrillator/Monitor M3538A Lithium Ion Batteries Revision J The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillation. The device is for use by qualified medical personnel trained in the operation of the device…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1097-2014·2014-03-05
Ossur Recalls Symbionic Leg Due to Battery Warning Failure
Ossur is recalling 144 Symbionic Leg prosthetics because they fail to display a low battery warning before powering down.
Product
The SYMBIONIC LEG is an integrated prosthetic leg for transfemoral and knee disarticulation amputees. Product Usage: SYMBIONIC LEG is intended for continuous use by amputees of low to moderate impact levels that weigh less than 125 kg for foot categories 25 30 and less…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1553-2014·2014-03-05
Popcorn Factory Recalls Heart-Shaped Popcorn Balls Due to Missing Allergen Labels
The Popcorn Factory is recalling heart-shaped popcorn balls because the Nutrition Facts and allergen labels were not applied to the individual pieces. The product contains milk and soy allergens.
Product
Candy coated popcorn shaped into a heart weighing 1.5 ounces per piece and individually wrapped in clear plastic packaging. There are 24 popcorn balls per case.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1099-2014·2014-03-05
Fresenius Optiflux F160NR Dialyzers Recalled for Dialysate Port Leak
Fresenius Medical Care is recalling Optiflux F160NR dialyzers because the dialysate port may leak during priming. The recall covers 6,720 units distributed in the US and Mexico.
Product
Optiflux F160NR High Flux Dialyzers; Product Number: 0500316N. Single Use acute or chronic hemanalysis treatment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1075-2014·2014-03-05
Radiometer D788 pCO2 Membranes Recalled for Biased Measurement Results
Radiometer America is recalling D788 pCO2 membranes because they may cause biased measurement results for patients and quality control.
Product
pCO2 D788 Membranes. Distributed by Radiometer America, Inc., Westlake, OH. An automatic or semi-automatic instrument used to identify and quantify two or more gases, and sometimes electrolytes, in whole blood using multiple special electrodes.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1079-2014·2014-03-05
Zimmer Recalls Trabecular Metal Reverse Shoulder System Due to Disassociation
Zimmer, Inc. is recalling 73,002 units of the Trabecular Metal Reverse Shoulder System because the Glenosphere can disassociate from the Baseplate.
Product
Trabecular Metal" Reverse Shoulder System
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1106-2014·2014-03-05
Fresenius Recalls Optiflux F18Nre Dialyzers Due to Port Leak Risk
Fresenius Medical Care is recalling 34,752 Optiflux F18Nre Flux Dialyzers because the dialysate port may leak during priming.
Product
Optiflux F18Nre Flux Dialyzers; Product Number: 0500308E. Single Use acute or chronic hemanalysis treatment.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1080-2014·2014-03-05
Siemens Artis zee Ceiling Systems Recalled for Cable Damage Risk
Siemens Medical Solutions USA is recalling 284 Artis zee Ceiling Systems due to potential cable damage from sub-optimal guidance.
Product
Siemens Artis zee Ceiling Systems. Angiographic x-ray system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1103-2014·2014-03-05
Fresenius Optiflux F200NR Dialyzers Recalled for Dialysate Port Leak
Fresenius Medical Care is recalling 19,596 Optiflux F200NR dialyzers due to a dialysate port leak during priming. The units were distributed in the US and Mexico.
Product
Optiflux F200NR High Flux Dialyzers; Product Number: 0500320N. Single Use acute or chronic hemanalysis treatment.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1567-2014·2014-03-05
Mars Recalls Uncle Ben's Saffron Rice Due to Mild Flushing Reports
Mars Food US is recalling Uncle Ben's Infused Rice Saffron Flavor after reports of mild flushing reactions that resolved within two hours.
Product
Uncle Ben's (R), Infused(R) Rice Saffron Flavor, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-11547
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1088-2014·2014-03-05
Actavis Recalls Subpotent Gelnique Oxybutynin Chloride Gel Samples
Actavis is recalling Gelnique (oxybutynin chloride) Gel 10% physician samples because drug potency was compromised during shipment.
Product
Gelnique (oxybutynin chloride) Gel 10%, 100 mg in 1 g sachet, for topical use only. Physician sample in clamshell container with seven heat-sealed sachets. Rx Only. Watson Pharmaceuticals Inc, Corona, CA, 92890. NDC: 52544-084-77.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1564-2014·2014-03-05
Mars Recalls Uncle Ben's Rice Due to Mild Flushing Reports
Mars Food US is recalling Uncle Ben's Infused Rice Roasted Chicken Flavor after reports of mild flushing reactions that resolved within two hours.
Product
Uncle Ben's (R), Infused(R) Rice Roasted Chicken Flavor, net weight 5 LB (2.27 kg) and 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1563-2014·2014-03-05
Mars Recalls Uncle Ben's Infused Rice Mexican Flavor Due to Flushing Reports
Mars Food US is recalling Uncle Ben's Infused Rice Mexican Flavor after reports of mild flushing reactions that resolved within two hours.
Product
Uncle Ben's (R), Infused(R) Rice Mexican Flavor, net weight 5 LB (2.27 kg) and 25 LB (11.34 kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1590-2014·2014-03-05
Mars Recalls Uncle Ben's Infused Rice Cheese Flavor Due to Flushing Reports
Mars Food US is recalling Uncle Ben's Infused Rice Cheese Flavor nationwide after reports of mild flushing reactions that resolved within two hours.
Product
Uncle Ben's (R), Infused(R) Rice Cheese Flavor, net weight 5 LB (2.27 kg), Distributed by MARS foodservices US, P.O. Box 11547, Carson, CA 90749-1547
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1087-2014·2014-03-05
Ortho VITROS Sodium Slides Recalled for False Positive Results
Ortho Clinical Diagnostics is recalling VITROS Na+ Slides and Calibrator Kit 2 because they may produce false positive sodium results in serum and plasma samples.
Product
VITROS Chemistry Products Na+ Slides, manufactured by Ortho Clinical Diagnostics 513 Technology Blvd Rochester, NY 14652 VITROS Na+ Slides quantitatively measure sodium (Na+) concentration in serum, plasma, and urine using VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1087-2014·2014-03-05
Actavis Recalls Clonazepam Tablets Due to Subpotent Tablet Weight
Actavis Elizabeth LLC is recalling 13,608 bottles of Clonazepam 2 mg tablets because routine testing found one tablet with weight below specification.
Product
Clonazepam Tablets, USP 2 mg 100 tablets Manufactured by: Actavis Elizabeth LLC 200 Elmora Avenue, Elizabeth, NJ 0737 USA NDC 0228-3005-11 packaged in White/Round HDPE 75 CC with white/round plastic 33 mm CRC closure shipped in corrugated 75 cc carton (24 bottles/carton)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1094-2014·2014-03-05
Hologic Recalls NovaSure Radiofrequency Controllers for Electrical Standard Non-Compliance
Hologic is recalling 93 NovaSure Radiofrequency Controllers because they may not meet the IEC 60601-1 electrical safety standard.
Product
NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency Controller, Model Number: 71978-001 Catalog Number: RFC2009 Product Usage: The NovaSure Impedance Controlled Endometrial Ablation System is intended to ablate the endometrial lining of the uterus in…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1076-2014·2014-03-05
Siemens Dimension Vista Enzyme 1 Calibrator Recalled for QC Shifts
Siemens Healthcare Diagnostics is recalling specific lots of Dimension Vista Enzyme 1 Calibrator due to quality control shifts and imprecision during Pseudocholinesterase calibration.
Product
Dimension Vista Enzyme 1 Calibrator (ENZ 1 CAL) lots 3FD034 and 3HD012. An in vitro diagnostic multi-analyte calibrator for the calibration of Amylase (AMY), Gamma-Glutamyl Transferase (GGT), Lactate Dehydrogenase (LDH), Lipase (LIPL), and Pseudocholinesterase (PCHE) methods…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1088-2014·2014-03-05
Ortho VITROS Chemistry Calibrator Kit 2 Recalled for False Positive Results
Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 2 because it may produce false positive serum and plasma sample results.
Product
VITROS Chemistry Products Calibrator Kit 2, manufactured by Ortho Clinical Diagnostics 1000 Lee Road Rochester, NY 14606 VITROS Chemistry Products Calibrator Kit 2 is used to calibrate VITROS 250/350/950/5,1 FS and 4600 Chemistry Systems and the VITROS 5600 Integrated System…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1068-2014·2014-03-05
Smith & Nephew Recalls Renasys EZ PLUS Canisters for Labeling Changes
Smith & Nephew is recalling Renasys EZ PLUS canisters to modify the bacterial overflow guard and update product labeling.
Product
Renasys EZ PLUS, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1067-2014·2014-03-05
Smith & Nephew Recalls Renasys EZ Canisters for Labeling and Filter Changes
Smith & Nephew is recalling Renasys EZ canisters to modify the bacterial overflow guard and update product labeling.
Product
Renasys EZ, a Canister Component of of Renasys EZ Negative Pressure Wound Therapy System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1565-2014·2014-03-05
Mars Recalls Uncle Ben's Garlic & Butter Rice Due to Flushing Reports
Mars Food US is recalling Uncle Ben's Infused Rice Garlic & Butter Flavor after reports of mild flushing reactions that resolved within two hours.
Product
Uncle Ben's (R), Infused(R) Rice Garlic & Butter Flavor, net weight 5 LB (2.27kg), Distributed by MARS foodservices US, P.O. Box 5059, Rancho Dominguez, CA 90224-5059
Category
Food
Distribution
Distributed nationwide