State

US Virgin Islands product recalls

73,509 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 39
Most recent: 2026-10-14

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25651–25675 of 73686

HighFDA (Devices)·Z-1160-2021·2021-03-10
United Imaging X-ray System Recalled for Uncommanded Motion Hazard
Shanghai United Imaging Healthcare is recalling six X-ray systems because the tube head may move unexpectedly, posing a collision risk to patients.
Product
Digitial Medica X-ray Imagining System, Model: uDR 596i, RX, CE0123, UDI:(01) 06971576833023 - Product Usage: intended to used by a qualified/trained doctor or technician on both adult and pediatric subjects for taking diagnostic radiographic exposures of the skull, spinal…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V157000·2021-03-10
2021 Porsche vehicles recalled for potentially loose suspension components
Porsche is recalling certain 2021 Taycan, 911, Cayman, Boxster, and 718 Spyder models because suspension components may not have been properly tightened and could loosen, potentially causing loss of vehicle control.
Product
PORSCHE — PORSCHE TAYCAN, redundant CAYMAN, redundant BOXSTER, 911
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V153000·2021-03-10
Mercedes-Benz Sprinter Recalled for Sliding Door Lock Defect
Daimler Vans USA is recalling 2019-2020 Mercedes-Benz Sprinter vans with optional electric sliding doors because the auxiliary lock may be the incorrect type, potentially increasing injury risk in a crash.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21E018000·2021-03-10
Safety Belt Solutions Recalls Seat Belts Due to Heat-Treatment Defect
Safety Belt Solutions is recalling specific seat belts because the tongues may not have been heat-treated correctly, potentially failing to restrain occupants in a crash.
Product
SEAT BELTS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V159000·2021-03-10
Audi passenger air bag may not deploy correctly in certain model years
Volkswagen Group (Audi) is recalling certain 2019-2021 Audi models for defective passenger air bags that may not deploy properly during a crash. Owners should contact Audi at 1-800-253-2834 for free inspection and repair.
Product
AUDI — AUDI A6, A7, A6 ALLROAD, S6
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1158-2021·2021-03-10
BioFire BCID2 Panel Recalled for False Positive Pseudomonas Results
BioFire Diagnostics is recalling BCID2 Panels due to a risk of false positive Pseudomonas aeruginosa results when used with specific BD BACTEC blood culture vials.
Product
BioFire BCID2 Panel; IVD, Rx Only Part No: RFIT-ASY-0147 / UDI: 00815381020338 - Product Usage: intended for use with FilmArray systems.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1151-2021·2021-03-10
Baxter Recalls PrisMax Hemodialysis Tubing Due to Performance Variability
Baxter Healthcare is recalling PrisMax System Version II hemodialysis tubing due to performance variability that may cause alarms and therapy interruptions.
Product
The PrisMax System Version II Hemodialysis Delivery System: Automatic Repositioning System Pump Assembly, specifically tubing, Model Numbers: a) 955626 b) 955558 c) 955701 PrisMax V2 Preventive Maintenance Kit, Product Code SC616 ARPS PUMP, Product Code SC6035 ARPS Pump…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V156000·2021-03-10
2021 BMW XB7, X5, and X7 Head Restraints May Detach in Crash
BMW is recalling certain 2021 XB7, X5, and X7 vehicles because the head restraints on second-row outer seats may be an incorrect type and could detach during a crash, increasing injury risk.
Product
BMW — BMW X7, XB7, X5, X5 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21092·2021-03-10
Lifetime Products Recalls 6-Foot Seminar Tables Due to Injury Risk
Lifetime Products is recalling 6-foot seminar tables because the brace arms may fail to lock, causing the table to collapse and posing an injury risk.
Product
Lifetime Products 6-foot Seminar Tables
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·21093·2021-03-10
Hillsdale Jennings Counter and Bar Stools Recalled for Fall Hazard
Hillsdale Furniture is recalling Jennings counter and bar stools because the seat can break off the base, posing a fall hazard.
Product
Hillsdale Furniture Jennings Counter and Bar Stools
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V161000·2021-03-10
2019-2021 Genesis G70 Engine Compartment Fire Risk from ABS Module
Hyundai is recalling 2019-2021 Genesis G70 vehicles because the Anti-Lock Brake System module could short-circuit and cause an engine compartment fire. Owners should park outside until the ABS module fuse is replaced.
Product
GENESIS — GENESIS G70
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1173-2021·2021-03-10
Siemens Sensis Vibe Systems Recalled for Potential System Freezes
Siemens is recalling 37 Sensis Vibe systems in the US because they may sporadically freeze during operation or idle, preventing user interaction.
Product
Sensis / Sensis Vibe systems with software version VD12 and equipped with HP Flex Pro-C PC. Diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies Model Numbers: Sensis Vibe Hemo 11007641 Sensis Vibe Combo 11007642 Sensis…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0297-2021·2021-03-10
Teva Recalls Metoclopramide Injection Due to Chemical Contamination
Teva Pharmaceuticals is recalling Metoclopramide Injection vials due to an unknown brown residue found inside one vial.
Product
METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0296-2021·2021-03-10
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system is out of specification for mechanical peel.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0294-2021·2021-03-10
Noven Recalls Daytrana Methylphenidate Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling 551,670 Daytrana methylphenidate patches nationwide because the delivery system failed mechanical peel specifications.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1153-2021·2021-03-10
Bovie Velocity Disposable Bipolar Ablators Recalled for Sterile Packaging Defect
Bovie Medical Corporation is recalling Velocity Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.
Product
Velocity Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1170-2021·2021-03-10
Boston Scientific Recalls Polypectomy Snares Due to Incomplete Pouch Seals
Boston Scientific is recalling Captivator, Captiflex, and Sensation polypectomy snares because users reported incomplete pouch seals before use.
Product
Captivator/Captiflex/Sensation Short Throw Single-Use Polypectomy Snares Outer box UPN, Inner pouch UPN: M00560311 (Box 5), M00560310; M00560321 (Box 5), M00560320; M00562651 (Box 5), M00562650; M00562652 (Box 20), M00562650; M00562671 (Box 5), M00562670…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0293-2021·2021-03-10
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling 473,280 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0295-2021·2021-03-10
Noven Recalls Daytrana Patches Due to Defective Delivery System
Noven Pharmaceuticals is recalling 786,900 Daytrana (methylphenidate) patches because the delivery system failed mechanical peel specifications.
Product
DAYTRANA — DAYTRANA (METHYLPHENIDATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1155-2021·2021-03-10
Bovie Medical Recalls ConMed Disposable Bipolar Ablators Due to Packaging Defect
Bovie Medical Corporation is recalling 5,270 ConMed Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the sterile barrier.
Product
ConMed Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0292-2021·2021-03-10
Dr. Reddy's Recalls Progesterone Capsules Due to Dissolution Failures
Dr. Reddy's Laboratories is recalling 16,449 bottles of 200 mg Progesterone Capsules because stability testing revealed out-of-specification dissolution results.
Product
PROGESTERONE — PROGESTERONE (PROGESTERONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1164-2021·2021-03-10
G & H Wire Company Recalls Orthodontic Elastic Bands Due to Labeling Error
G & H Wire Company is recalling orthodontic elastic bands because the patient pack text is incorrect, which could lead to misuse and temporary discomfort.
Product
Band, Elastic, Orthodontic - Product Usage: Orthodontic elastics, also referred to as rubber bands, are small stretchy loops of rubber that help move teeth into proper alignment during orthodontic treatment. Their purpose is to create additional force for tooth movement in any…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1154-2021·2021-03-10
Bovie Medical Recalls HNM Disposable Bipolar Ablators Due to Packaging Defect
Bovie Medical Corporation is recalling 3,862 HNM Disposable Bipolar Ablators because pinholes in the sterile packaging may compromise the barrier.
Product
HNM Disposable Bipolar Ablators - Product Usage: intended to be used for cutting, vaporization, and coagulation of soft tissue during arthroscopic surgical procedures.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1163-2021·2021-03-10
Johnson & Johnson Recalls Nonconforming TECNIS Toric Intraocular Lenses
Johnson & Johnson Surgical Vision Inc is recalling 27 TECNIS Toric 1-Piece Intraocular Lenses due to the release of nonconforming products.
Product
TECNIS Toric 1-Piece IOL, Model Number: ZCT150 +23.5D SE 1.50D CYL - Product Usage: intended to be placed in the capsular bag.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1152-2021·2021-03-10
CooperSurgical Recalls Milex Gellhorn Flexible Pessaries Due to Manufacturing Error
CooperSurgical is recalling specific lots of Milex Gellhorn Flexible pessaries because they were manufactured with incorrect stem lengths.
Product
Milex Gellhorn Flexible under the following labels: 1) Gellhorn Flexible w/Short Stem Pessary, REF MXKPGSS2-1/4, 2-1/4" (57 mm) with Kit, 2) Gellhorn Flexible w/Short Stem Pessary, REF MXPGSS2-1/4, 2-1/4" (57 mm) without Kit, 3) Gellhorn Flexible w/Short Stem Pessary, REF…
Category
Medical Device
Distribution
Distributed nationwide