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.

59501–59525 of 74011

HighFDA (Devices)·Z-0915-2014·2014-02-12
GE Healthcare Recalls Infant Resuscitation Units Due to Loose Adjustment Knob
GE Healthcare is recalling 48 Stand-Alone Resuscitation Units because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture delivered to patients.
Product
Stand-Alone Resuscitation Unit, Bag and Mask, Upgrade Kits, part number M1139612, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com*** Provides the basic equipment required for pulmonary resuscitation of infant.s
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·14V071000·2014-02-12
Three Feathers Recalls Trailers With Defective Door Locks
Three Feathers is recalling 480 trailers equipped with Fastec door locks that may jam, potentially trapping occupants inside.
Product
THREE FEATHERS — THREE FEATHERS MULE CARGO HAULER, PELICAN CARGO HAULER, PINECONE TEAR DROP TRLR, TUMBLEWEED CAMPER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0929-2014·2014-02-12
Siemens Recalls ADVIA Centaur Phenytoin Calibrator Due to Recovery Changes
Siemens Healthcare Diagnostics is recalling specific lots of ADVIA Centaur Phenytoin Calibrator N because a change in recovery was observed compared to previous lots.
Product
ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 2-pack SMN 10311391 For in vitro diagnostic use in the quantitative determination of phenytoin in serum or plasma using the ADVIA Centaur and ADVIA Centaur XP systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0914-2014·2014-02-12
GE Healthcare Recalls Infant Resuscitation Units Due to Loose Adjustment Knob
GE Healthcare is recalling 15 infant resuscitation units because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture.
Product
Stand-Alone Resuscitation Unit, Bag and Mask, part number M1226444, labeled in part ***GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com***. Provides the basic equipment required for pulmonary resuscitation of infants.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·14105·2014-02-12
MAT Industries Recalls HDX and Powermate Air Compressors Due to Shock Hazard
MAT Industries is recalling HDX and Powermate two-gallon air compressors because pressure switch terminals can contact the motor housing, posing a shock hazard.
Product
HDX™ and Powermate® two-gallon air compressors
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·14V054000·2014-02-12
Toyota Recalls 2012-2013 RAV4, Tacoma, and RX350 for Electronic Stability Control Defect
Toyota is recalling specific 2012-2013 RAV4, Tacoma, and RX350 vehicles because an electrical component in the brake actuator may fail, causing safety systems to stop working.
Product
TOYOTA — TOYOTA, LEXUS RAV4, TACOMA, RX350
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1078-2014·2014-02-12
Sheffield Pharmaceuticals Recalls Dollar General Triple Antibiotic Ointment for Microbial Contamination
Faria Limited LLC is recalling Dollar General Triple Antibiotic Ointment due to elevated counts of gram-positive rods found during environmental testing.
Product
Dollar General Triple Antibiotic Ointment; NET WT 1 OZ (28 g), OTC, DISTRIBUTED BY DOLGENCORP LLC, GOODLETTSVILLE, TN 37072
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·14V072000·2014-02-12
R&M Trailer Recalls 2012-2013 Enclosed Cargo Trailers Due to Door Lock Defect
R&M Trailer is recalling 185 model year 2012-2013 enclosed cargo trailers because a door lock defect could jam the deadbolt, potentially trapping occupants inside.
Product
R&M TRAILER — R&M TRAILER 6X12 ENCLOSED CARGO, 7X16 ENCLOSED CARGO
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0913-2014·2014-02-12
GE Healthcare Panda Infant Warmers Recalled for Loose Adjustment Knob
GE Healthcare is recalling Panda iRes and Freestanding Infant Warmers because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture delivered to patients.
Product
Panda iRes¿ Infant Warmers, part number M1112198 and Panda Freestanding Warmers, part number 2063568, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com** Panda Infant Warmers provide infrared heat in a controlled manner to neonates who…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0928-2014·2014-02-12
Elekta XiO RTP System Recalled for Incorrect Effective Depth Calculation
Elekta, Inc. is recalling 1,424 XiO RTP Systems because the software may calculate incorrect Effective Depth values when bolus is present.
Product
XiO RTP System. Used to create treatment plans for any cancer patient for whom external beam radiation therapy or brachytherapy has been prescribed.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0911-2014·2014-02-12
GE Healthcare Recalls X-ray Systems Due to Monitor Suspension Nut Issue
GE Healthcare is recalling Precision 500D, MPI, and RXI X-ray systems because a locking nut on the overhead monitor suspension may loosen.
Product
GE Healthcare Precision 500D, Precision MPI & Precision RXI X-ray imaging systems. The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0912-2014·2014-02-12
GE Healthcare Recalls Giraffe Infant Warmers Due to Loose Adjustment Knob
GE Healthcare is recalling 1,970 Giraffe Infant Warmers because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture delivered to patients.
Product
Giraffe¿ Infant Warmers, part number M1118179, labeled in part *** GE Healthcare 8880 Gorman Road Laurel, MD 20723***www.gehealthcare.com* Giraffe¿ Infant Warmers provide infrared heat in a controlled manner to neonates who are unable to thermo-regulate based on their own…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0916-2014·2014-02-12
GE Healthcare Recalls Stand-Alone Resuscitation T-Pieces Due to Loose Knob
GE Healthcare is recalling 375 Stand-Alone Resuscitation T-Pieces because a loose adjustment knob may affect the accuracy of the blended Air/Oxygen gas mixture delivered to patients.
Product
Stand-Alone Resuscitation, T-Piece, part numbers 2063771-001, 2063772-001, 2063773-001, 2063774-001, 2063775-001, M1226442, M1241420, M1241421, M1241424, M1241425, M1241427, M1241430, M1241461, M1241463, M1241464, and M1241589; labeled in part ***GE Healthcare 8880 Gorman Road…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0907-2014·2014-02-12
Siemens SOMATOM CT Systems Recalled for Potential Display Freeze Malfunction
Siemens Medical Solutions is recalling 147 SOMATOM CT systems due to a potential display freeze malfunction during clinical operation.
Product
Siemens SOMATOM Definition, Definition AS, Definition Flash, and Definition Edge systems. X-ray tomography, computed, radiology.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1056-2014·2014-02-12
Insight Instruments Recalls Cornea Coat Hydroxypropylmethylcellulose Syringes
Insight Instruments is recalling Cornea Coat syringes because they were marketed without an approved NDA or ANDA.
Product
Cornea Coat, Hydroxypropylmethylcellulose, 1.5ml Syringe, Rx Only. Manufactured by: Insight Instruments, Inc., 2580 SE Willoughby Blvd., Stuart, FL 34994, USA. Tel: 772-219-9393.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0920-2014·2014-02-12
Fresenius Bicarbonate Jug Adapter Recalled for Premature Distribution
Fresenius Medical Care is recalling 703 Bicarbonate Jug Adapters distributed before receiving FDA 510(k) approval.
Product
Fresenius Bicarbonate Jug Adapter to the 2008 Series Hemodialysis machine Part Number: 650103. The adapter is a socket that accepts the 2008 machine spike to draw concentrate from the container.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0930-2014·2014-02-12
Siemens Recalls ADVIA Centaur Phenytoin Calibrator Due to Recovery Changes
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Phenytoin Calibrator N lots due to observed changes in assay recovery.
Product
ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 6-pack SMN 10314977 For in vitro diagnostic use in the quantitative determination of phenytoin in serum or plasma using the ADVIA Centaur and ADVIA Centaur XP systems
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1074-2014·2014-02-12
Teva Recalls Hydralazine HCL Tablets Due to Impurity Concerns
Teva Pharmaceuticals USA is recalling specific lots of Hydralazine HCL 25 mg tablets because they may contain impurities outside of specification limits.
Product
Hydralazine HCL Tablets, USP, 25 mg in a single blister package, Manufactured in Czech Republic By: Teva Czech Industries s.r.o. Opava-Komarov, Czech Republic, Distributed by Goldline Laboratories, Sellersville, PA, NDC 00182-0554-89 (carton) and 00182-0554-00 (single blister).
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1075-2014·2014-02-12
Teva Recalls Hydralazine HCL Tablets Due to Impurity Concerns
Teva Pharmaceuticals USA is recalling specific lots of Hydralazine HCL 50 mg tablets because they may fail impurity specifications throughout their shelf life.
Product
Hydralazine HCL Tablets, USP, 50 mg in a single blister package, Rx only, Manufactured in Czech Republic by: Teva Czech Industries s.r.o. Opava-Komarov, Czech Republic, Distributed by Goldline Laboratories, Sellersville, PA, NDC 00182-0555-89 (carton) and 00182-0555-00 (single…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1076-2014·2014-02-12
Sheffield Triple Antibiotic Ointment Recalled for Microbial Contamination
Sheffield Pharmaceuticals is recalling Sheffield Triple Antibiotic Ointment due to elevated counts of gram-positive rods found during environmental testing.
Product
SHEFFIELD TRIPLE ANTIBIOTIC — SHEFFIELD TRIPLE ANTIBIOTIC (BACITRACIN ZINC, POLYMYXIN B SULFATE, NEOMYCIN SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0903-2014·2014-02-12
Stryker Neptune 2 Rover Ultra Waste Management System Field Upgrade
Stryker is upgrading Neptune 2 Rover Ultra Waste Management Systems in the field to meet new 510(k) clearance specifications.
Product
Neptune 2 Rover Ultra Waste Management System
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0933-2014·2014-02-12
Stryker Recalls Gaymar Medi-Therm Devices Due to Missing Water Temperature Display
Stryker is recalling 1,002 Gaymar Medi-Therm devices because the water temperature display is blank in Auto mode, potentially preventing users from verifying water temperature.
Product
The Gaymar Medi-Therm device provides a means of regulating patient temperature by supplying temperature-controlled water through a connector hose to accessory Gaymar Hyper/Hypothermia blanket(s)/body wrap(s). The blanket/body wrap provides an interface for heating or cooling…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1060-2014·2014-02-12
Actavis Recalls Diclofenac Sodium and Misoprostol Tablets Due to Broken Tablets
Actavis Inc is recalling 6,540 bottles of Diclofenac Sodium and Misoprostol tablets because some tablets are broken.
Product
DICLOFENAC SODIUM AND MISOPROSTOL — DICLOFENAC SODIUM AND MISOPROSTOL (DICLOFENAC SODIUM AND MISOPROSTOL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1077-2014·2014-02-12
FAMILY wellness Triple Antibiotic Ointment Recalled for Microbial Contamination
Faria Limited LLC is recalling FAMILY wellness Triple Antibiotic Ointment due to elevated counts of gram-positive rods found during environmental testing.
Product
FAMILY wellness Triple Antibiotic Ointment. NET WT 1 OZ (28 g), OTC, DISTRIBUTED BY: FAMILY DOLLAR SERVICES, INC., MATTHEWS,NC 28105
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0904-2014·2014-02-12
Horiba Medical Recalls ABX PENTRA N Control for Revised Potassium Values
Horiba Medical is recalling ABX PENTRA N Control units because the product was updated to include a revised Target Value assignment for Potassium.
Product
ABX PENTRA N Control, Model No. A11A01653 The ABX PENTRA N Control is for use in quality control by monitoring accuracy and precision for the quantitative methods as specified in the enclosed annex.
Category
Medical Device
Distribution
Distributed nationwide