State

US Virgin Islands product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

53376–53400 of 74002

ModerateFDA (Devices)·Z-1928-2015·2015-07-08
Roche LDL-Cholesterol Test Recalled for Potential Drug Interference
Roche Diagnostics is recalling 6,255 units of the LDL-Cholesterol plus gen.2. test due to potential false results caused by drug interference.
Product
LDL-Cholesterol plus gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test in intended for the quantitative determination of low-density lipoprotein Cholesterol (LDL-C) in serum and plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1957-2015·2015-07-08
Siemens CentraLink Data Management System Software Recall
Siemens recalls CentraLink software because the sample query function may fail to return all samples from Dimension Vista systems under specific configurations.
Product
CentraLink" Data Management System; software is a network solution provider and multi-system data manager for the instruments and lab automation systems (LAS) within the lab. The CentraLink software consolidates data from all connected instruments so that an operator can review…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1869-2015·2015-07-08
Covidien Recalls Palindrome Precision SI Chronic Catheter Kits
Covidien LLC is recalling Palindrome Precision SI Chronic Catheter Kits because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome Precision SI Chronic Catheter Kit w/VenaTrac Stylet 14.5 Fr x 19cm Item Code: 8888145062CP
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1927-2015·2015-07-08
Roche LDL-Cholesterol Test Recalled for Potential Drug Interference
Roche Diagnostics is recalling the LDL-Cholesterol gen.2 test because certain drugs may cause falsely decreased results when using the Trinder reaction method.
Product
LDL-Cholesterol gen.2. The Boehringer Mannheim Direct LDL-Cholesterol test in intended for the quantitative determination of low-density lipoprotein Cholesterol (LDL-C) in serum and plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1915-2015·2015-07-08
DePuy Synthes Titanium Recon Screws Recalled for Incorrect Insert
Synthes, Inc. is recalling 276 DePuy Synthes 6.5 mm Titanium Recon Screws because certain lots contain the wrong insert.
Product
DePuy Synthes 6.5 mm Titanium Recon Screws w/T25 Stardrive (70mm, 75mm, 80mm, 85mm, 90mm, 95mm, 105mm); part of the Expert Lateral Femur Nail System and indicated to stabilize Subtrochanteric fractures, Ipsilateral neck/shaft fractures, Femoral shaft fractures, Impending…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1946-2015·2015-07-08
Axis-Shield Homocysteine Reagent Recalled for Performance Deterioration
Axis-Shield Diagnostics is recalling Liquid Stable 2-Part Homocysteine Reagents due to performance deterioration that causes under-recovery of test results.
Product
Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT; 100 test format, 1000 test format, and 200 test format; and Private Label: (Distributed by BECKMAN COULTER, for professional use only, on the BECKMAN COULTER AU platforms (AU400, AU480, AU680 and AU5800)) Product…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1882-2015·2015-07-08
Palindrome SI Chronic Catheters Recalled for Antimicrobial Specification Failure
Covidien LLC is recalling Palindrome SI Chronic Catheters because they may not meet antimicrobial specifications. The recall affects units with expiry dates of February 2018 and earlier.
Product
Palindrome SI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 28cm Item Code: 8888128458
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1920-2015·2015-07-08
Roche Cholesterol Reagent Recalled for Potential Drug Interference
Roche Diagnostics is recalling Cholesterol CHOD-PAP reagents because drug interference may cause falsely decreased test results.
Product
Cholesterol CHOD-PAP. In vitro diagnostic reagent system intended for use on the Hitachi systems for The quantitative determination of total cholesterol in serum and plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1960-2015·2015-07-08
Spine Wave Access Kit Recalled for Mislabeled Probe Dimensions
Spine Wave, Inc. is recalling 121 Spine Wave Access Kits because the outer carton mislabels the monopolar probe dimensions. The probe is listed as 200 x 1.5mm instead of the correct 280 x 1.5mm.
Product
Spine Wave Access Kit, Catalog Number 10-1530 Package contents: RLSP494-Rhythmlink Monopolar Stimulating Probe and 10-1525 Disposable Dilator Set. Product Usage: The Spine Wave Access Kit is comprised of a sterile monopolar stimulating probe (individually packaged by…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1921-2015·2015-07-08
Roche Cholesterol Gen.2 Cassette Recalled for Potential Drug Interference
Roche Diagnostics is recalling Cholesterol Gen.2 cassettes because Trinder reaction tests may yield falsely decreased results when specific drugs are present.
Product
Cholesterol Gen.2. The cassette COBAS Integra Cholesterol Gen.2 (CHOL2) contains an in vitro diagnostic reagent system intended for use on COBAS Integra 800 and 400 plus systems, cobas c111, and cobas c systems for the quantitative determination of total cholesterol in serum…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1967-2015·2015-07-08
Tecan Infinite F500 Microplate Reader Recalled for Firmware Bug
Tecan US, Inc. is recalling 868 Infinite F500 microplate readers because a firmware bug causes incorrect luminescence values to be displayed.
Product
Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with injector option. The Infinite F500 provides high performance for the vast majority of todays microplate applications and research and is robotic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1924-2015·2015-07-08
Roche HDL-Cholesterol gen.3. Recalled for Potential Drug Interference
Roche Diagnostics is recalling HDL-Cholesterol gen.3. reagents due to potential false results caused by drug interference on Cobas Analyzers.
Product
HDL-Cholesterol gen.3. For the quantitative determination of high-density lipoprotein Cholesterol (HDL-C) in serum and plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1206-2015·2015-07-08
Takeda Recalls Contrave Tablets Due to Broken or Split Defects
Takeda Pharmaceuticals is recalling 3,619 bottles of Contrave extended-release tablets due to potential tablet defects, including broken tablets and equatorial splitting.
Product
CONTRAVE (naltrexone HCl and bupropion HCl )extended-release tablets, 8 mg/ 90 mg, 120-count bottle, Rx only, Manufactured for Orexigen Therapeutics, Inc., La Jolia, CA 92037, Distributed by Takeda Pharmaceuticals America, Inc., Deerfield, IL 60015, NDC 64764-890-99.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1970-2015·2015-07-08
Tecan Infinite 200 PRO Microplate Reader Recalled for Firmware Bug
Tecan US, Inc. is recalling 868 Infinite 200 PRO microplate readers because a firmware bug causes incorrect luminescence values to be displayed.
Product
Infinite 200 PRO in vitro diagnostic. Product Usage: The Tecan Infinite 200 PRO is a multifunctional microplate reader with injector option. The Infinite 200 PRO provides high performance for the vast majority of todays microplate applications and research and is robotic…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1926-2015·2015-07-08
Roche Lactate Reagent Recalled for Potential Drug Interference
Roche Diagnostics is recalling Lactate reagent due to potential false results caused by drug interference with the Trinder reaction method.
Product
Lactate. Intended for use on COBAS INTEGRA 800 and 400 plus systems, cobas c111, Roche/Hitachi MODULAR systems, and cobas c systems for the quantitative determination of lactate concentration in plasm and cerebrospinal fluid.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1971-2015·2015-07-08
Tecan Infinite 200 Microplate Reader Recalled for Firmware Bug
Tecan US, Inc. is recalling 868 Infinite 200 microplate readers because a firmware bug causes incorrect luminescence values to be displayed.
Product
Infinite 200 in vitro diagnostic. Product Usage: The Tecan Infinite 200 is a multifunctional microplate reader with injector option. The Infinite 200 provides high performance for the vast majority of todays microplate applications and research and is robotic compatible.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1925-2015·2015-07-08
Roche HDL-Cholesterol Reagent Recalled for Potential Drug Interference
Roche Diagnostics is recalling HDL-Cholesterol plus gen.3. reagents due to potential false results when used with certain drugs.
Product
HDL-Cholesterol plus gen.3.; and Small Supersized Intended for use on COBAS Integra 800 and 400 plus systems, cobas c111, and cobas c systems for the quantitative determination of HDL-cholesterol concentration in serum and plasma.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D1151-2015·2015-07-08
Qualitest Recalls Disulfiram Tablets Due to Dissolution Failure
Qualitest Pharmaceuticals is recalling 2,016 bottles of Disulfiram tablets because one lot failed routine stability testing for dissolution specifications.
Product
Disulfiram tablets, USP, 500 mg, 100-count bottles, Rx only, Manufactured for and by Qualitest Pharmaceuticals 130 Vintage Drive Huntsville, AL 35811. NDC 0603-3432-21.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1907-2015·2015-07-08
Palindrome HSI Chronic Catheter Recall for Antimicrobial Specification Failure
Covidien LLC is recalling Palindrome HSI Chronic Catheters because they may not meet antimicrobial specifications. The recall affects 72,363 units in the US and 24,631 internationally.
Product
Palindrome HSI Chronic Catheter Sport Pack w/VenaTrac Stylet 14.5 Fr x 33cm Item Code: 8888133509
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1940-2015·2015-07-08
Alcon Accurus Vitreous Probes Recalled for Packaging Seal Defect
Alcon Research is recalling Accurus vitreous probes due to insufficient outer packaging seals that may compromise sterility.
Product
Accurus 2500 Standalone Vitreous Probe REF 8065741018; Accurus 23 GA Standalone Vitreous Probe REF 8065750821; Accurus 25+ 2500 CPM Standalone Vitreous Probe REF 8065751122; Anterior Accurus Probe with Infusion Needle REF 8065803650; Single Use Sterile Probes Rx only.…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1931-2015·2015-07-08
Roche Uric Acid Plus Test Recalled for Drug Interference
Roche Diagnostics is recalling Uric Acid plus ver.2 tests because results may be falsely decreased when used with certain drugs.
Product
Uric Acid plus ver.2 In vitro test for the quantitative determination of uric acid in human serum, plasma and urine or Roche/Hitachi MODULAR systems, cobas c111, COBAS Integra 800 and 400 plus systems, and cobas c systems.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·15V431000·2015-07-07
Dodge Journey Recall: Engine Cover May Detach and Cause Fire
Chrysler is recalling 2011-2015 Dodge Journey vehicles because the engine cover may detach and contact the exhaust manifold, increasing the risk of a vehicle fire.
Product
DODGE — DODGE JOURNEY
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·098-2015·2015-07-07
Bassett and Walker Recalls Beef Lips Lacking Import Inspection
Bassett & Walker International is recalling approximately 1,540 pounds of beef lip products produced in Australia that were not inspected at the U.S. point of entry.
Product
Bassett and Walker International, Inc. Recall Beef Products Produced Without Benefit of Import Inspection
Category
Food
Distribution
Distributed nationwide
HighNHTSA·15V432000·2015-07-07
Thomas Built Buses Recall Emergency Door Handle Corrosion Defect
Daimler Trucks North America is recalling 103,038 Thomas Built Buses because corrosion on the emergency door handle stem could delay evacuation during an emergency.
Product
THOMAS — THOMAS, THOMAS BUILT BUSES SAF-T-LINER CONVENTIONAL, SAF-T-LINER C2, SAF-T-LINER FS65, SAF-T-LINER HDX
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·15V433000·2015-07-07
Ferrari Recalls 2015 Models Due to Driver Air Bag Assembly Defect
Ferrari is recalling 814 model year 2015 vehicles because an improperly assembled driver air bag module may deploy in a rotated orientation, increasing injury risk in a crash.
Product
FERRARI — FERRARI F12 BERLINETTA, LAFERRARI, 458, CALIFORNIA T
Category
Vehicle
Distribution
Distributed nationwide