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.

60051–60075 of 74011

HighFDA (Devices)·Z-0520-2014·2013-12-25
Intuitive Surgical Recalls Mega Needle Drivers for Potential Jaw Detachment
Intuitive Surgical is recalling Mega Needle Drivers for the da Vinci S and Si systems due to a potential risk of jaw insert detachment.
Product
Mega Needle Driver, 8MM assembly of the da Vinci S IS1200 and da Vinci Si, IS2000. Manufactured by Intuitive Surgical, Sunnyvale, CA. EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1126-2014·2013-12-25
Senor Murphy Candymaker Recalls Chocolate Pretzels for Undeclared Allergens
Senor Murphy Candymaker is recalling Chocolate Pretzels and other confections due to undeclared allergens. Consumers should stop using the products.
Product
Senor Murphy Santa Fe Candymaker Chocolate Pretzels 3 oz.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0545-2014·2013-12-25
ASI Medical Recalls SEAC Advanced Dental Systems Due to Air Tank Rupture Risk
ASI Medical is recalling 337 SEAC Advanced Dental Systems because the miniature plastic air tank can potentially rupture.
Product
SEAC Advanced Dental System, Model A591561 The SEAC Advanced Dental System is a self-contained dental delivery system with a built-in air compressor,vacuum system and water supply. It is designed operate dental handpiece attachments and suction instruments. The SEAC Advanced…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1124-2014·2013-12-25
Senor Murphy Candymaker Recalls Multiple Candies for Undeclared Allergens
Senor Murphy Candymaker is recalling eight candy products due to undeclared allergens. Consumers should stop eating these items and check the recall list.
Product
Senor Murphy Santa Fe Candymaker Cashew Crunch , 4oz and 1 lb. Handmade with cashews, sugar, corn syrup, butter, soda, and salt.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0522-2014·2013-12-25
Mobility Unlimited Recalls KayserBetten IDA Beds Due to Door Joint Failure
Mobility Unlimited Inc. is recalling 33 KayserBetten model IDA beds because door joints may loosen or separate, causing doors to drop outward and potentially injure users.
Product
KayserBetten model IDA beds Product Usage: BED, AC-POWERED ADJUSTABLE HOSPITAL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0517-2014·2013-12-25
Siemens Recalls Dimension TACR Flex Reagent Cartridges for Stability Issues
Siemens is recalling Dimension TACR Flex reagent cartridges because reduced stability may cause inaccurate test results for transplant patients.
Product
Dimension(R) TACR Flex(R) reagent cartridge (DF107) The TACR method is an in vitro diagnostic test intended to quantitatively measure Tacrolimus in human whole blood on the Dimension(R) clinical chemistry system. Measurements of Tacrolimus are used as an aid in the management…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1128-2014·2013-12-25
Senor Murphy Candymaker Recalls Multiple Confections for Undeclared Allergens
Senor Murphy Candymaker is recalling eight confection products due to undeclared allergens. Consumers should stop eating these items and return them to the point of purchase.
Product
Senor Murphy Santa Fe Candymaker Pinon Brittle , 4 oz and 1 lb. Handmade with pinones (pine nuts), sugar, corn syrup, butter, soda, and salt.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0521-2014·2013-12-25
Intuitive Surgical Recalls Large Needle Drivers Due to Jaw Insert Detachment Risk
Intuitive Surgical is recalling Large Needle Drivers for the da Vinci S and Si systems because the jaw insert may detach during use.
Product
Large Needle Driver, 8MM assembly of the da Vinci S IS1200 and da Vinci Si, IS2000. Manufactured by Intuitive Surgical, Sunnyvale, CA. EndoWrist Instruments, including scissors, scalpels, forceps, needle drivers and electrocautery are intended for endoscopic manipulation…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0537-2014·2013-12-25
Remel Inc Recalls Streptex Kits Due to Potential False Negative Results
Remel Inc is recalling 768 Streptex kits because they may produce weak or false negative test results for Streptococcal grouping.
Product
Streptex* kit, Ref R30950501 ZL50, Rapid latex test for Streptococcal grouping, IVD. The kit contains reagent groups A, B, C, D, F, G, a control, and an extraction enzyme. The firm name on the label is Remel Europe Ltd., Dartford, England. Streptex is a rapid latex test…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1127-2014·2013-12-25
Senor Murphy Candymaker Recalls Multiple Products for Undeclared Allergens
Senor Murphy Candymaker is recalling eight candy products due to undeclared allergens. The recall covers nationwide distribution.
Product
Senor Murphy Santa Fe Candymaker Chile Peanuts, 4 and 9 oz. Handmade with peanuts, sugar, corn syrup, brown sugar, butter, baking soda, Shimayo red chile, and salt.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1123-2014·2013-12-25
Senor Murphy Candymaker Recalls Pecan Bueno for Undeclared Allergens
Senor Murphy Candymaker is recalling Pecan Bueno and other products due to undeclared allergens. Consumers should stop eating these items.
Product
Senor Murphy Santa Fe Candymaker Pecan Bueno, 4oz and 1 lb. Handmade with pecans, sugar, corn syrup, butter, soda, and salt.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0518-2014·2013-12-25
Kimberly-Clark Epidural Pain Management Trays Recalled for Syringe Defect
Kimberly-Clark is recalling Single Shot Epidural Pain Management Trays because the included BD LOR Syringes may stall or stick.
Product
Kimberly-Clark Single Shot Epidural Pain Management Trays containing the BD LOR Syringe (BD Code 405198) Product Usage: The device is designed to provide regional anesthesia. The device may contain syringes, needles and drugs
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1129-2014·2013-12-25
Senor Murphy Candymaker Recalls Multiple Confections for Undeclared Allergens
Senor Murphy Candymaker is recalling eight confection products due to undeclared allergens. The recall covers nationwide distribution.
Product
Senor Murphy Santa Fe Candymaker Peanut Brittle , 4 oz and 1 lb.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0525-2014·2013-12-25
Ortho-Clinical Diagnostics Recalls VITROS CA 125 II Calibrators
Ortho-Clinical Diagnostics is recalling VITROS CA 125 II Calibrators due to a positive shift in patient results.
Product
VITROS CA 125 II Calibrators For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, VITROS 3600 Immunodiagnostic System and VITROS 5600 Integrated System for the quantitative measurement of OC 125 defined antigen in human serum and plasma (EDTA or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0533-2014·2013-12-25
Integra Epidural Anesthesia Kits Recalled Due to Syringe Plunger Defect
Integra LifeSciences is recalling specific lots of epidural anesthesia kits because the included BD LOR syringe plunger may stall or stick.
Product
Integra Disposable, Convenience Kit Single Shot Epidural Tray Reorder Number 340269 Rx Only Product Usage: The Integra kits which contain a BD LOR syringe are intended to provide licensed medical professionals with a kit containing drugs and other medical devices that are…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1125-2014·2013-12-25
Senor Murphy Candymaker Recalls Chocolate Products Due to Undeclared Allergens
Senor Murphy Candymaker is recalling multiple chocolate and nut products because they contain undeclared allergens.
Product
Senor Murphy Santa Fe Candymaker Chile Pistachio Bark , 2.5 oz and 1 lb. Handmade with dark chocolate (sugar, chocolate liquor processed with alkali, cocoa butter, milk fat, soy lecithin - an emulsifier, natural flavors), pistachios, chile, salt.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-1100-2014·2013-12-25
Source Naturals Essential Enzyme Ultra Recalled for Chloramphenicol Contamination
Source Naturals Essential Enzyme Ultra is being recalled because it was made with bulk products containing chloramphenicol.
Product
Source Naturals Essential Enzyme Ultra VEGI-CAP: Premium Digestive Enzyme Blend; 30, 60, 90 & 120 count bottles. Vegetarian capsules Manufactured for: Source Naturals, Inc. Santa Cruz, CA
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0768-2014·2013-12-25
National Enzyme Recalls Carbgestkosh Capsules Due to Chloramphenicol Contamination
National Enzyme Co is recalling bulk Carbgestkosh capsules because they may contain chloramphenicol levels exceeding 0.3 ppb.
Product
Bulk 9809 ENZYMEDICA CARBGESTKOSH capsules, packaged in poly bags in corrugated boxes (for domestic distribution) or fiber drums (for international distribution) (SKU 92103).
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0496-2014·2013-12-25
Stryker Neurovascular Microcatheters Recalled for Shelf-Life Labeling Errors
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with 'use by' dates exceeding available shelf-life data.
Product
Stryker brand EXCELSIOR SL-10 PRE-SHAPED C 15OCM; Catalog Number: M0031441940; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Stryker Neurovascular, Fremont, CA Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0546-2014·2013-12-25
Arrow International Recalls Nerve Block Catheter Kits Due to Labeling Error
Arrow International is recalling 121 Continuous Peripheral Nerve Block Catheter Kits because the packaging incorrectly describes the stimulator cable connector.
Product
Continuous Peripheral Nerve Block Catheter Kit and Set Continuous Peripheral Nerve Block Catheter Kit and Set permits placement of catheters next to nerves and nerve plexuses for continuous nerve block anesthesia or analgesia techniques for periods not exceeding 72 hours.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0785-2014·2013-12-25
National Enzyme Recalls Dietary Supplements Due to Chloramphenicol Contamination
National Enzyme Co is recalling specific dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Product
Dietary Supplements packaged in the following configuration: (1) NEC Healthy Pre Menopausal, Feminine Support for Active Women, packaged in 60-capsule bottles (SKU 54389). Firm name on the label is National Enzyme Company, Forsyth, MO; (2) Root 86, Healthy Pre Menopausal…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0746-2014·2013-12-25
National Enzyme Co Recalls Dietary Supplements Due to Chloramphenicol Contamination
National Enzyme Co is recalling specific dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
Product
Dietary Supplement packaged in the following configurations: (1) 5357 NWC UltraEnzSup 90' packaged in 90 count capsule unlabeled bottles (SKU 50027); (2) 5357 NWC UltraEnzSup UNL 200 packaged in 200 count capsule unlabeled bottles (SKU 50028); (3) NWC Naturals Ultra Enzyme…
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0744-2014·2013-12-25
National Enzyme Recalls Blue-Green Algae Supplements Due to Chloramphenicol
National Enzyme Co is recalling Applied Health blue-green algae supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
Product
Applied Health, Solutions for Life, Foundation Blue-Green Algae, Detoxify and Regenerate Energy and Immune Booster, Daily Essential Nutrients packaged in 90-capsule bottles (SKU 53623). Firm name on the label is Applied Health Solutions, Scottsdale, AZ.
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0810-2014·2013-12-25
National Enzyme Recalls PerformanceZyme Supplements Due to Chloramphenicol Contamination
National Enzyme Co is recalling PerformanceZyme dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
Product
PerformanceZyme, packaged 250-capsule bottles (SKU 54825) and 120-capsule bottles (SKU 54826). Norwegian label;
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0506-2014·2013-12-25
Stryker Neurovascular Microcatheters Recalled for Incorrect Use-By Dates
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
Product
Stryker brand COMPLIANT 4MM X 15MM, Catalog Number: M003SRC04150; Product is manufactured by Stryker Neurovascular, Cork, Ireland and distributed by Excelsior SL-10/Excelsior 1018 Microcatheter: Stryker Neurovascular Microcatheters are intended to assist in the delivery of…
Category
Medical Device
Distribution
Distributed nationwide