State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

58326–58350 of 74005

HighFDA (Devices)·Z-1658-2014·2014-06-04
Siemens ADVIA Centaur Vitamin D Test Recalled for Fluorescein Interference
Siemens Healthcare Diagnostics is recalling 40,266 ADVIA Centaur Systems VitD Total 100 test kits because samples containing fluorescein may interfere with the assay results.
Product
ADVIA Centaur Systems VitD Total 100 test, Ready Pack, For OUS; SMN 10699201. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-1350-2014·2014-06-04
Sandoz Recalls Cefpodoxime Proxetil Tablets Due to Stainless Steel Particles
Sandoz, Inc. is recalling Cefpodoxime Proxetil tablets because they contain stainless steel particles. The recall covers 22,818 bottles distributed nationwide.
Product
CEFPODOXIME PROXETIL — CEFPODOXIME PROXETIL (CEFPODOXIME PROXETIL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1669-2014·2014-06-04
Synthes ProDisc-C Milling Bits Recalled Due to Breakage Risk
Synthes, Inc. is recalling specific lots of ProDisc-C 2.0mm Milling Bits because they have an increased potential to break during use.
Product
Synthes ProDisc-C 2.0mm Milling Bit, Synthes 2.0mm Milling Bit HXC, Synthes 2.0mm Milling Bit with 2.35mm x 33.5mm Shaft, and Synthes 2.0mm Milling Bit with Flat Coupling. Spinal surgical instrument: The Synthes ProDisc-C 2.0mm Milling Bits are used as a part of the milling…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1664-2014·2014-06-04
Beaver-Visitec Anterior Chamber Cannula Recalled for Sharp Tip Needle
Beaver-Visitec International Inc. is recalling Visitec Anterior Chamber Cannulas because some units contain a sharp tip needle instead of a blunt tip cannula.
Product
Visitec Anterior Chamber Cannula, .40x22mm (27Gx7/8in) REF 585006 Cannulae are intended to irrigate and or aspirate ophthalmic solutions and liquids in or out of the eye, and remove materials where appropriate. These products are used in all sections of the eye. This cannula…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1652-2014·2014-06-04
Siemens Linear Accelerator Recall for Unvalidated Stereotactic Accessories
Siemens Medical Solutions is recalling nine Linear Accelerator units because they may be used with unvalidated stereotactic accessories.
Product
Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray radiation for therapeutic treatment of cancer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1654-2014·2014-06-04
Siemens ADVIA Centaur TSH3 Ultra Reagent Recall Due to Interference
Siemens is recalling ADVIA Centaur TSH3 Ultra reagent kits because samples containing fluorescein may interfere with test results.
Product
ADVIA Centaur Systems TSH3 Ultra , Ready Pack, 500 test Catalog Number: 06491080; Siemens Material Number: 10282379. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1666-2014·2014-06-04
B. Braun Recalls Sprotte Spinal Needles Missing Introducer Needles
B. Braun Medical is recalling 24-gauge Sprotte Spinal Needles and Trays because the accompanying introducer needles are missing.
Product
Sprotte Spinal Tray / Sprotte Spinal Needle 24 gauge with Introducer Spinal injection of anesthetics to provide regional anesthesia
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1655-2014·2014-06-04
Siemens ADVIA Centaur TSH3 Ultra Recalled for Fluorescein Interference
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Systems TSH3 Ultra kits because fluorescein samples may interfere with test results.
Product
ADVIA Centaur Systems TSH3 Ultra 2500 tests Catalog Number: 04862625; Siemens Material Number (SMN) : 10361944. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1656-2014·2014-06-04
Siemens ADVIA Centaur VitD 100 Test Recalled Due to Fluorescein Interference
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Systems VitD 100 test kits because fluorescein samples may interfere with assay results.
Product
ADVIA Centaur Systems VitD 100 test, Ready Pack, Catalog Number: 10491994. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1665-2014·2014-06-04
GE Healthcare Recalls Centricity PACS Workstation Due to Image Rejection Error
GE Healthcare is recalling 297 Centricity PACS Workstations because a software defect may cause images from previously displayed studies to be rejected unintentionally.
Product
The Centricity PACS Workstation is intended for use as a primary diagnostic and analysis tool for diagnostic images by trained healthcare professional, including radiologists, physicians, technologists, clinicians, and nurses. It is also intended for use as a clinical review…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1657-2014·2014-06-04
Siemens ADVIA Centaur VitD 500 Test Recalled for Fluorescein Interference
Siemens is recalling ADVIA Centaur VitD 500 test kits because fluorescein samples may interfere with assay results.
Product
ADVIA Centaur Systems VitD 500 test, Ready Pack, Catalog Number: 10631021. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1659-2014·2014-06-04
Siemens Recalls ADVIA Centaur BRAHMS PCT 100 Test Kits Due to Interference
Siemens Healthcare Diagnostics is recalling 16,302 ADVIA Centaur BRAHMS PCT 100 test kits because samples containing fluorescein may interfere with assay results.
Product
ADVIA Centaur Systems BRAHMS PCT 100 test Sold only OUS; Catalog Number: 10378883.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1668-2014·2014-06-04
Siemens ACUSON SC2000 Ultrasound Systems Recalled for Software Malfunction
Siemens is recalling 177 ACUSON SC2000 ultrasound systems due to a software issue in the Stress Echo feature that may require studies to be repeated.
Product
ACUSON SC2000 Ultrasound Systems with software version 3.5 (VA35) and using Stress Echo Feature. Ultrasound imaging system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1355-2014·2014-06-04
Wockhardt Recalls Metoprolol Succinate Extended-Release Tablets Due to Dissolution Failure
Wockhardt USA LLC is recalling 8,712 bottles of Metoprolol Succinate Extended-Release Tablets, 100 mg, because they failed dissolution testing.
Product
Metoprolol Succinate Extended-Release Tablets, USP, 100 mg, 100-count bottle, Rx only. Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC., 20 Water view Blvd., Parsippany, NJ 07054, USA. NDC: 64679-736-02.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1653-2014·2014-06-04
Siemens Recalls ADVIA Centaur TSH3 Ultra Ready Packs Due to Interference
Siemens Healthcare Diagnostics is recalling ADVIA Centaur TSH3 Ultra Ready Packs because samples containing fluorescein may interfere with assay results.
Product
ADVIA Centaur Systems TSH3 Ultra Ready Pack, 100 test Catalog Number: 06491072; Siemens Material Number: 10282378. Intended for the invitro diagnostic use in quantitative determination of various assays on the ADVIA Centaur and ADVIA Centaur XP analyzers.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1353-2014·2014-06-04
PediaCare Day & Night Cold Syrup Recalled for Precipitate
Prestige Brands Holdings is recalling PediaCare Day & Night Cold syrup bottles due to the presence of precipitate.
Product
PediaCare brand DAY & NIGHT Value Pack DAYTIME MULTI-SYMPTOM Cold (dextromethorphan HBr 5 mg and Phenylephrine HCl 2.5 mg) and NIGHTTIME MULTI-SYMPTOM Cold (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL oz (118 mL) bottles, one each of DAYTIME MULTI-SYMPTOM…
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1352-2014·2014-06-04
PediaCare Nighttime Cold Syrup Recalled for Diphenhydramine Precipitate
Prestige Brands Holdings is recalling PediaCare Nighttime Multi-Symptom Cold syrup due to the presence of diphenhydramine precipitate in the solution.
Product
PediaCare brand NIGHTTIME MULTI-SYMPTOM Cold, (diphenhydramine HCl 6.25 mg and phenylephrine HCl 2.5 mg), 4 FL OZ (118 mL), Distributed by Medtech Products, Inc., Tarrytown,NY ---- UPC 814832013544
Category
Drug
Distribution
Distributed nationwide
HighCPSC·14197·2014-06-03
Mission Archery Recalls MXB Crossbows Due to Unexpected Firing Hazard
Mission Archery is recalling about 9,500 MXB crossbows because they can fire unexpectedly without the trigger being pulled, posing an injury risk.
Product
MXB crossbows
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14V291000·2014-06-02
Jaguar Recalls 2013-2014 XF Models Due to Brake Pipe Wear
Jaguar is recalling 2013-2014 XF vehicles because the rear brake pipe may wear and leak fluid, increasing crash risk.
Product
JAGUAR — JAGUAR XF
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14E035000·2014-06-02
Roush Propane Fuel System Conversion Kits Recalled for Leak Risk
Roush CleanTech is recalling propane fuel system conversion kits for Ford vans due to a potential leak at the fuel line fitting that could cause a fire.
Product
FUEL SYSTEM, OTHER recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V292000·2014-06-02
Jaguar Recalls 2013 XJ Vehicles Due to Airbag Software Defect
Jaguar is recalling 2013 XJ vehicles because generic software in the Restraints Control Module may prevent the airbag system from operating correctly, increasing injury risk in a crash.
Product
JAGUAR — JAGUAR XJ
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V289000·2014-05-30
Kia Recalls 2014 Cadenza Vehicles Due to Wheel Fracture Risk
Kia is recalling 2014 Cadenza vehicles with 19-inch non-chrome aluminum wheels because they may fracture from impacts, increasing crash risk.
Product
KIA — KIA CADENZA
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14E028000·2014-05-29
Ford Recalls All-Weather Floor Mats for Interference with Accelerator Pedal
Ford is recalling all-weather driver-side floor mats for 2006-2011 Ford, Mercury, and Lincoln vehicles because they may shift and interfere with the accelerator pedal.
Product
LINCOLN — LINCOLN, MERCURY, FORD MKZ, MILAN, FUSION, ZEPHYR
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·14196·2014-05-29
Trident Recalls Pool UV Sanitation Systems Due to Fire Hazard
Trident is recalling Series 2 ultraviolet pool sanitation systems because electrical arcing can cause them to catch fire. Consumers should unplug the units and contact Trident for a free repair kit.
Product
Trident Series 2 Ultraviolet Sanitation Systems for pools
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·14V286000·2014-05-29
Ford Recalls 2011-2013 Explorers for Electric Power Steering Defect
Ford is recalling 2011-2013 Explorers because an intermittent connection in the electric power steering gear can cause a loss of power steering assist, increasing crash risk.
Product
FORD — FORD EXPLORER
Category
Vehicle
Distribution
Distributed nationwide