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.

59151–59175 of 74011

ModerateFDA (Devices)·Z-1148-2014·2014-03-12
GE Healthcare GSI Viewer Software Recall for Inaccurate Line Measurements
GE Healthcare is recalling GSI Viewer software because changing the region of interest or zooming may result in inaccurate line measurements.
Product
GE Healthcare, Model Number/ Description: 5342114 GSI Viewer 1.10 on AW VolumeShare 4 (AW 4.5); 5342114-2 GSI Viewer 1.10 on AW VolumeShare 4 (AW 4.5); 5342114-3 GSI Viewer 1.10 on AW VolumeShare 4 (AW 4.5); 5342114-4 GSI Viewer 1.11 on AW VolumeShare 4 (AW 4.5)…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1132-2014·2014-03-12
Mako Surgical Recalls Restoris Multicompartmental Knee System Due to Mislabeling
Mako Surgical Corporation is recalling 41 units of the Restoris Multicompartmental Knee System because the product may be mislabeled, which could result in the incorrect implant being used.
Product
Restoris Multicompartmental Knee (MCK) System is an implant system designed to be used with MAKO's Robotic Arm Interactive Orthopedic System (RIO). It is composed of a unicompartmental implant system (Restoris MCK Uni) and a patellofemoral implant system (Restoris MCK PF). The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1146-2014·2014-03-12
Horiba Medical Recalls ABX PENTRA Calibrators Due to Updated Target Values
Horiba Medical is recalling ABX PENTRA calibrators and controls because target values for the Creatinine Rate Blank Method were updated.
Product
ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Control. The ABX PENTRA 400 and PC200 are benchtop clinical chemistry analyzers using two measuring principals: absorbance and ion selective electrodes. The ABX PENTRA Multical is a lyophilized human serum calibrator…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0973-2014·2014-03-12
Medtronic O-arm Imaging System Recalled for Labeling Compliance Gaps
Medtronic is recalling O-arm Imaging Systems because a review found gaps in compliance with FDA labeling requirements for user information.
Product
Medtronic O-arm Imaging System Mobile X-ray system. Model No. BI-700-00027 and BI-700-00028 The 0-arm Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging and is intended to be used where a physician benefits from 2D and 3D information of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1125-2014·2014-03-12
Synthes 5.0mm Variable Locking Screw Recalled for Incorrect Package Insert
Synthes, Inc. is recalling 45 units of 5.0mm Variable Locking Screws because one package contained the wrong insert.
Product
Synthes 5.0mm Variable Locking Screw This device is part of the Variable Angle Locking Compression Plate family and this technology included variable angle Combi holes in the plate shaft.The variable angle Combi hole provides the flexibility of axial compression and variable…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1123-2014·2014-03-12
AMO TECNIS CL Foldable Silicone IOLs Recalled for Incorrect Diopter Labeling
AMO Puerto Rico Manufacturing is recalling 169 units of TECNIS CL Foldable Silicone IOLs because they may be labeled with the incorrect diopter power.
Product
AMO TECNIS CL Foldable Silicone IOL with OptiEdge Design, Model Z9002, diopter size: 16.0 and 21.0. Indicated for primary implantation for the visual correction of aphakia in adult patients.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1142-2014·2014-03-12
KCI Recalls Prevena Customizable Dressing Due to Connector Difficulty
KCI USA is recalling 20,850 units of Prevena Customizable Dressing 5-Packs because the tubing connector is difficult to attach to the canister.
Product
PRE2055US: Prevena Customizable Dressing 5-Pack (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 environment and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1130-2014·2014-03-12
DJO Surgical Recalls Mispackaged Acetabular Liners for Hip Replacement
DJO Surgical is recalling 10 units of FMP X-alt Acetabular Liners that were mistakenly packaged and labeled as different models and sizes.
Product
FMP X-alt Acetabular Liner This acetabular liner is intended for use with DJO Surgical hip systems. It is used with an acetabular shell to replicate the kinematics of a natural hip.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1093-2014·2014-03-12
Teva Recalls Hydroxyzine Pamoate Capsules Due to Unapproved Manufacturing Material
Teva Pharmaceuticals USA is recalling 2,494 bottles of Hydroxyzine Pamoate Capsules, 100 mg, because the active ingredient was incorrectly released for use.
Product
HYDROXYZINE PAMOATE — HYDROXYZINE PAMOATE (HYDROXYZINE PAMOATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1094-2014·2014-03-12
Teva Recalls Dextroamphetamine Tablets Due to CGMP Deviations
Teva Pharmaceuticals is recalling specific lots of Dextroamphetamine tablets because they were manufactured using unapproved material and not properly quarantined.
Product
DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE — DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE (DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE AND AMPHETAMINE SULFATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1135-2014·2014-03-12
KCI Prevena Peel and Place System Kit Recalled for Connector Issues
KCI USA is recalling Prevena Peel and Place System Kits because the male tubing connector is difficult to connect to the female canister connector.
Product
PRE1001: Prevena Peel and Place System Kit 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 environment and removing exudates…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1065-2014·2014-03-12
Elekta Digital Accelerators Recalled for Default Value Reset Issues
Elekta, Inc. is recalling 472 digital accelerators because customers are resetting default values outside recommended factory settings.
Product
All Elekta digital accelerators with electrons and beam modulator, MLCi/MLCi2, Agility or Asymmetric Heads Product Usage: Deliver of radiation to defined target volumes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1146-2014·2014-03-12
Dr. Reddy's Recalls Lansoprazole Capsules Due to Microbial Contamination
Dr. Reddy's is recalling multiple brands of Lansoprazole Delayed Release Capsules due to out-of-specification microbial counts.
Product
a) Walgreens Lansoprazole Delayed Release Capsules, USP 15 mg/Acid Reducer, 14 capsules per Bottle, Dist by Walgreen Company, 200 Wilmot RD Deerfield IL 60015 b) Family Wellness Lansoprazole Delayed Release Capsules, USP 15 mg/Acid Reducer, 14 capsules per Bottle, Distributed…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1144-2014·2014-03-12
Focus Diagnostics Recalls Simplexa Flu and RSV Assay Kits
Focus Diagnostics is recalling Simplexa Flu A/B & RSV Direct Assay Kits due to the potential for false positive test results.
Product
Simplexa Flu AlB & RSV Direct Assay Kits, intended for use as an aid in the differential diagnosis of influenza A, influenza B, and RSV viral infections in humans and is not intended to detect influenza C. Model Number MOL2650.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1126-2014·2014-03-12
Hospira Recalls LifeShield Blood Sets Due to Assembly Errors
Hospira Inc. is recalling specific lots of LifeShield Latex-Free HEMA Y-Type Blood Sets because they were assembled incorrectly.
Product
*** 1) List number 126970465 labeled in part: 12697-65 LifeShield LATEX-FREE HEMA; Y-TYPE BLOOD SET, Nonvented, 88 Inch with 210 Micron Filter Pump, Prepierced Injection Site and Secure Lock; Made in Costa Rica; Product Inquiries should be directed to Hospira, Inc., Lake Forest…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1140-2014·2014-03-12
KCI USA Recalls Prevena Customizable Dressing 5-Pack Due to Connector Issue
KCI USA is recalling 20,850 units of the Prevena Customizable Dressing 5-Pack because the male connector on the tubing is difficult to connect to the female connector on the canister tubing.
Product
PRE2055: Prevena Customizable Dressing 5-Pack 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 environment and removing…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1136-2014·2014-03-12
KCI USA Recalls Prevena Peel and Place System Kits
KCI USA is recalling Prevena Peel and Place System Kits because the tubing connector is difficult to connect to the canister.
Product
PRE1001US: Prevena Peel and Place System Kit (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 environment and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1139-2014·2014-03-12
KCI Recalls Prevena Incision Management System Kits Due to Connector Issues
KCI USA is recalling Prevena Incision Management System kits because the male tubing connector is difficult to attach to the female canister connector.
Product
PRE2001: Prevena Incision Management Customizable System Box 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 environment and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1137-2014·2014-03-12
KCI Recalls Prevena Dressing Kits Due to Connector Connection Issues
KCI USA is recalling 20,850 Prevena Dressing kits because the male tubing connector is difficult to connect to the female canister connector.
Product
PRE1055: Prevena Dressing, 5 Pack 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 environment and removing exudates via the…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1092-2014·2014-03-12
Teva Recalls Ethambutol Hydrochloride Tablets Due to Incorrect Excipient
Teva Pharmaceuticals is recalling specific lots of Ethambutol Hydrochloride Tablets because they were manufactured with an unapproved gelatin excipient.
Product
Teva Ethambutol Hydrochloride Tablets, USP, 400 mg, 100- count bottle, Rx Only,Distributed by Teva Pharmaceuticals, USA, Sellersville, PA., NDC 0555-0923-02.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1133-2014·2014-03-12
BencoDental Tartar and Stain Remover Recalled for Incorrect Labeling
Heraeus Kulzer is recalling BencoDental tartar and stain remover due to incorrect labeling on the immediate container.
Product
BencoDental tartar & stain remover ultrasonic cleaning solution Product Usage: Formulated especially for removal of calculus, tartar, tobacco and food stains from dentures, bridges, orthodontic appliances, etc. Use also for removal of permanent cement.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1138-2014·2014-03-12
KCI Recalls Prevena Dressing Kits Due to Connector Connection Difficulty
KCI USA is recalling 20,850 Prevena Dressing kits because the tubing connector is difficult to connect to the canister.
Product
PRE1055US: Prevena Dressing, 5 Pack (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 environment and removing…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1113-2014·2014-03-12
Toshiba CT Systems Recalled for X-Ray Output Software Defect
Toshiba is recalling 338 Aquilion CT systems because a software defect may prevent X-ray exposure from starting during contrast studies.
Product
TSX-101A Aquilion 32/64 ONE Computed Tomography X-Ray System; TXS-101/R Aquilion RXL Computed Tomography X-Ray System; TSX-301A Aquilion One Computed Tomography X-Ray System; TSX-301B Aquilion Premium Computed Tomography X-Ray System; TSX-302A Aquilion Prime Computed Tomography…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1149-2014·2014-03-12
Medefil Recalls Heparin Syringes Due to Incorrect Barcode Labeling
Medefil Incorporated is recalling Heparin I.V. Flush Syringes because the barcodes on the master cartons do not match the printed product codes.
Product
Heparin I.V. Flush Syringe is available is pre-filled polypropylene syringes, 100 units/mL, 3 mL fill in a 12 mL syringe.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1097-2014·2014-03-12
Aaron Industries Recalls Tussin CF Cold Liquid Due to Precipitate
Aaron Industries is recalling Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid due to the presence of a white precipitate, confirmed to be the active ingredient guaifenesin.
Product
Tussin CF Adult Maximum Strength Multi-Symptom Cold liquid (dextromethorphan HBr 10 mg, guaifenesin 200 mg, phenylephrine HCl 5 mg) per 5 mL, 8 FL OZ (237 mL) bottle, Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716, NDC 49035-229-08, UPC 6 81131 03884 3.
Category
Drug
Distribution
Distributed nationwide