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.

60801–60825 of 74011

SevereFDA (Devices)·Z-0267-2014·2013-11-27
Medtronic Thunder Steerable Guidewire Recalled for Coating Delamination Risk
Medtronic Vascular is recalling 1,205 Thunder Steerable Guidewires because the PTFE coating may delaminate and detach from the device.
Product
THUNDER¿ Steerable Guidewire; Model: LVTNDR190S Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary and peripheral vasculature, and may be used to reach and cross a target…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-011-2014·2013-11-27
Greenstone Recalls Spironolactone Tablets Due to Unapproved Manufacturing Site Change
Greenstone LLC is recalling 4,848 bottles of Spironolactone 50 mg tablets because the manufacturing site change resulted in an unapproved dissolution profile.
Product
Spironolactone tablets, USP 50 mg, Rx only, 100 count bottle, Distributed By: Greenstone LLC, Peapack, NJ 07977, NDC: 59762-5012-1
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0265-2014·2013-11-27
Medtronic Vascular Recalls Attain Hybrid Guide Wires Due to Coating Defect
Medtronic Vascular is recalling 1,674 Attain Hybrid Guide Wires because the PTFE coating may delaminate and detach from the device.
Product
ATTAIN HYBRID¿ Guide Wire; Models: GWR419478, GWR419488, GWR419688 The Attain Hybrid guide wire is intended to aid in the placement of Medtronic transvenous left ventricular leads in the coronary vasculature.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0215-2014·2013-11-27
New Algae Company Recalls EDGE Dietary Supplement for Undeclared Shark Cartilage
New Algae Company is recalling EDGE dietary supplement packets because the label fails to declare shark cartilage. The product was distributed nationwide.
Product
EDGE, Item number 21-620, dietary supplement, 60 packet per box. The Edge product includes two different packets of capsules - a "Before" packet and an "After" packet. The suggested use for the After packet is one packet (or 6 capsules) per day. The suggested use for…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0262-2014·2013-11-27
Medtronic Zinger Guidewires Recalled for Coating Delamination Risk
Medtronic Vascular is recalling Zinger Stainless Steel Workhorse Guidewires because the PTFE coating may delaminate and detach.
Product
Zinger¿ Stainless Steel Workhorse Guidewire; Models: ZNGRLS180HJ, ZNGRLS180HS, ZNGRMS180HJ, ZNGRMS180HS, ZNGRMS180S, ZNGRS180HJ, ZNGRS180HS, ZNGRS180S Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0266-2014·2013-11-27
Medtronic Cougar Steerable Guidewires Recalled for Coating Delamination Risk
Medtronic Vascular is recalling 20 units of Cougar Steerable Guidewires because the PTFE coating may delaminate and detach.
Product
COUGAR¿ Steerable Guidewire; Models: LVCLS190J, LVCLS190S, LVCXT190J, LVCXT190S Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary and peripheral vasculature, and may be…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0348-2014·2013-11-27
Candela Laser GentleLase Pro Recalled for Unintended Pulse Emission Risk
Candela Corporation is recalling 1,258 GentleLase Pro laser surgical instruments because they may emit an unintended single pulse before the trigger is pressed, posing an injury risk.
Product
Candela Laser GentleLase Pro, Powered Laser Surgical Instrument for dermatological use - Model number: 9914-00-9015. and Candela Laser GentleLase Pro LE, Model number: 9914-00-9040
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0370-2014·2013-11-27
FDA Recalls Medcare Max-500 Patient Lifts Due to Potential Load Failure
Ergosafe Products LLC is recalling 97 Medcare Max-500 patient stands because the lift might fail with the labeled 500-lb load rating.
Product
Medcare Products Max-500 Stand, Total Support, patient stand, model #400006. The responsible firm name listed in the Operations Manual is Medcare Products, Burnsville, MN. Used for assisting patients/residents to a standing position.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-015-2014·2013-11-27
Affirm XL Nutritional Supplement Recalled for Unapproved Sildenafil Analogue
Affirm XL is recalling its nutritional supplement because FDA analysis found it contains sulfoaildenafil, an unapproved analogue of sildenafil.
Product
Affirm XL Nutritional Supplement, 1 and 10 count blister packs and single pill packs, Manufactured by Dongseo Biopharm Corp., Yongin City, Kyonggi do, Korea, distributed by: Affirm XL, LLC, Ladera Ranch, CA
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0264-2014·2013-11-27
Medtronic ProVia Crossing Guidewire Recalled for Coating Delamination Risk
Medtronic Vascular is recalling ProVia Crossing Guidewires because the PTFE coating may delaminate and detach from the device.
Product
ProVia¿ CROSSING GUIDEWIRE; Models: 15PROV300HS, 3PROV180HS, 3PROV180SS, 3PROV300HS, 3PROV300SS, 9PROV180HS, 9PROV180SS Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0263-2014·2013-11-27
Medtronic Thunder Extra Support Guidewire Recalled for Coating Delamination Risk
Medtronic Vascular is recalling 58 Thunder Extra Support Guidewires because the PTFE coating may delaminate and detach from the device.
Product
THUNDER¿ Extra Support Guidewire; Models: THNDR190J, THNDR190S, THNDR300J, THNDR300S Medtronic guide wires are steerable guide wires that are used for the introduction and placement of diagnostics or interventional devices in the coronary and peripheral vasculature, and may…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0218-2014·2013-11-27
Terri Lynn Deluxe Mixed Nuts Recalled for Undeclared Peanuts
Terri Lynn Inc. is recalling Deluxe Mixed Nuts with Macadamia because the bags contain undeclared peanuts, posing a risk to people with peanut allergies.
Product
Mixed nuts in a plastic bag labeled in part: Deluxe Mixed Nuts with Macadamia; NET WT. 12 OZ. (340 g), 30 LB, 35 LB; P.O. BOX 5118 ELGIN, IL 60121
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-012-2014·2013-11-27
Hospira Recalls Metoclopramide Injection Due to Glass Particulate Matter
Hospira Inc. is recalling 251,400 vials of Metoclopramide Injection because glass spicules were found during a site inspection.
Product
METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0216-2014·2013-11-27
Flex Dietary Supplement Recalled for Undeclared Shark Cartilage
New Algae Company is recalling Flex dietary supplement bottles because the label fails to declare shark cartilage, a potential allergen.
Product
Flex, Maximum Flexibility, Item number 21-601, dietary supplement, 90 capsules per bottle. The Flex product is a dietary supplement in capsule form containing vegetable glucosamine HCL, chondroitin sulfate (shark cartilage), organic microalgae (aph. flos-aquae) and chicken…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-013-2014·2013-11-27
Hospira Recalls Ondansetron Injection Vials Due to Glass Spicules
Hospira Inc. is recalling 681,400 vials of Ondansetron Injection because glass spicules were found during a site inspection.
Product
ONDANSETRON — ONDANSETRON (ONDANSETRON)
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Food)·F-0177-2014·2013-11-27
Bio-Cat Recalls Pectinase Enzyme Blends Due to Chloramphenicol Contamination
Bio-Cat Inc is recalling bulk pectinase enzyme blends intended for food and dietary supplement manufacturing because they may be contaminated with chloramphenicol.
Product
Pectinase Enzyme Blends, bulk, custom blended formulations identified as pectinase 500, pectinase 1000, Pectinase 350 Endo-pg/gm, PC Blend 14, Nut 14-500, pectinase 3500, gastro blend 0111, Digestive Blend 021894, enzyme complex 5763, pectinase 1750, pectinase 350, EC-CHPX…
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0352-2014·2013-11-27
Spacelabs recalls anesthesia workstation absorbers due to potential switch failure
Spacelabs Healthcare is recalling CAS I/II Absorbers for Blease anesthesia workstations because the Bag-to-Vent switch may fail due to loose hardware.
Product
CAS I/II Absorbers that are parts of the BleaseSirius Anesthesia Workstation, the BleaseFocus Anesthesia Workstation with the following part numbers: 12200900; 12200901; 12200902; 12200903; 14200100, and service kits part number 050-0659-00 and 050-0901-00. BleaseFocus…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0178-2014·2013-11-27
Bio-Cat Recalls Xylanase Enzyme Blends Due to Chloramphenicol Contamination
Bio-Cat Inc is recalling bulk xylanase enzyme blends intended for food and dietary supplement manufacturing due to potential chloramphenicol contamination.
Product
Xylanase Enzyme Blends, bulk, custom blended formulations identified as xylanase 1000, xylanase 150,000 XU, synerzyme-ae, brizyme, Cellulase Special Blend OMRI, xylanase amylase blend, Bio-Cat Ruminant Enzyme, Feed Blend ws alkacel 20x, BC-XR, enzyme blend #2237, CHX blend…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0343-2014·2013-11-27
Siemens ADVIA 1200 Software Recalled for Ration Parameter Flagging Errors
Siemens Healthcare Diagnostics is recalling ADVIA 1200 System Software versions 2.00 and 2.01 due to incorrect ration parameter flagging behavior.
Product
ADVIA 1200 System Software: 1) V2.00, 2) V2.01. Performs assays for general and specialty chemistries, methods for specific protein measurement, drugs-of-abuse testing and therapeutic drug monitoring.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0345-2014·2013-11-27
Siemens ADVIA Chemistry System Software Recalled for Parameter Flagging Errors
Siemens Healthcare Diagnostics is recalling ADVIA 1800 System Software V2.01 due to ration parameters flagging behavior issues.
Product
ADVIA 1800 System Software V2.01. Performs assays for general and specialty chemistries, methods for specific protein measurement, drugs-of-abuse testing and therapeutic drug monitoring.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0191-2014·2013-11-27
Guzzler Concord Grape Beverage Recalled for Potential Cap Fragment Ingestion
American Beverage Corp is recalling Guzzler Concord Grape beverages because a part of the nozzle cap may dislodge and be ingested.
Product
Guzzler Concord Grape 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0196-2014·2013-11-27
Guzzler Orchard Chill bottles recalled due to potential cap dislodgement hazard
American Beverage Corp is recalling Guzzler Orchard Chill bottles because the nozzle cap may dislodge if chewed, posing a choking or ingestion risk.
Product
Guzzler Orchard Chill, 20 fl. oz. PET plastic bottle with a sports cap, American Beverage Corporation, Verona PA.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0204-2014·2013-11-27
American Beverage Corp. Recalls Big Hug Fruit Barrel Citrus Bottles
American Beverage Corp. is recalling Big Hug Fruit Barrel Citrus bottles due to a potential choking hazard from dislodged nozzle cap parts.
Product
Big Hug Fruit Barrel Citrus in a 16 oz plastic bottle with a sports cap, American Beverage Corp., Verona PA.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0209-2014·2013-11-27
American Beverage Corp. Recalls Big Burst Grape Drink Due to Cap Hazard
American Beverage Corp. is recalling Big Burst Grape Drink because a part of the nozzle cap could become dislodged and ingested, posing a health hazard.
Product
Big Burst Grape Drink in a 16 oz PET plastic bottle with a sports cap, American Beverage Corp., Verona PA.
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0189-2014·2013-11-27
American Beverage Corp. Recalls Big Hug Fruit Barrel Orange Bottles
American Beverage Corp. is recalling Big Hug Fruit Barrel Orange bottles due to a potential risk of nozzle cap parts becoming dislodged and ingested.
Product
Big Hug, Fruit Barrel Orange in a plastic 16 oz bottle with a sports cap, American Beverage Corp., Verona, PA.
Category
Food
Distribution
Distributed nationwide