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.

56576–56600 of 74005

ModerateFDA (Drugs)·D-0083-2015·2014-11-05
Martin Avenue Pharmacy Recalls Histamine Injectable Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Histamine 0.55 mg/mL injectable vials because quality control observations during an FDA inspection raised concerns about sterility assurance.
Product
Histamine 0.55 mg/mL injectable packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0128-2015·2014-11-05
Siemens Recalls ADVIA Centaur Ferritin Calibrator C Due to Analytical Sensitivity Issues
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Ferritin Calibrator C kits due to realignment issues with specific kit lots. The recall affects 8,263 kits distributed worldwide.
Product
ADVIA Centaur Ferritin Calibrator C-Used with the ADVIA Centaur Ferritin assay on the ADVIA Centaur CP system only. (In-Vitro Diagnostic) Catalog Number: 03439230 (2 pack)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0145-2015·2014-11-05
Parker Eclipse Probe Covers Recalled for Incorrect Expiration Date Labeling
Parker Laboratories is recalling Eclipse Probe Covers due to incorrect expiration dates on inner boxes and plastic bags.
Product
Parker Eclipse Probe Cover, Latex Free, REF 38-01, 10 Eclipse Probe Covers, Size: 2.37/1.75"W x 9.5"L (60/44 mm x 241 mm), Lot #D424, Expiry date 04/2016, Pre-gelled inside with Aquasonic 100 Ultrasound Transmission Gel Product Usage: For use as a protective cover for…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0166-2015·2014-11-05
Martin Avenue Pharmacy Recalls Tri-mix T25 Injectable Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Tri-mix T25 injectable vials because quality control observations during an FDA inspection presented a risk to sterility assurance.
Product
Tri-mix T25, 4.413 mg/0.145 mg/1.475 mcg/mL (papaverine, phentolamine mesylate, alprostadil) injectable packaged in a clear glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0153-2015·2014-11-05
Zimmer Dental Recalls Spline Twist Implants Due to Labeling Error
Zimmer Dental is recalling 1,044 Spline Twist Implants because the incorrect diameter size was printed on the inner vial.
Product
Spline Twist Implant, HA 3.25mmD X 15mmL; Part No. 2135. Zimmer Dental Spline implant systems are designed for use in edentulous mandibles or maxillae for attachment of complete denture prostheses for immediate or conventional loading, or as a terminal or intermediary…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0154-2015·2014-11-05
Zimmer Dental Recalls Tapered Screw-Vent Implants Due to Labeling Error
Zimmer Dental is recalling specific Tapered Screw-Vent Implants because the incorrect diameter size was printed on the inner vial.
Product
Tapered Screw-Vent Implant, MTX, 4.1mmD X 10mmL X 3.5mm Platform Part No. TSV4B10 Tapered Screw-Vent Implant, MTX, 4.1mmD X 11.5mmL X 3.5mm Platform Part No. TSV4B11 The Tapered Screw-Vent Implants are designed for use in the maxilla or mandible for immediate loading or…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0131-2015·2014-11-05
Abbott Lipase Reagent Recalled for Incorrect Package Insert Parameters
Abbott Laboratories is recalling Lipase Reagent 7D80 because package inserts contain incorrect SmartWash parameters for Triglyceride.
Product
Lipase Reagent, 7D80. Used to measure lipase in human serum on the Architect system.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0147-2015·2014-11-05
CooperSurgical Recalls Blunt Hurd Cannula Due to Incorrect Package Insert
CooperSurgical is recalling 90 units of Blunt Hurd Cannula because the wrong package insert was included in the shipping materials.
Product
Blunt Hurd Cannula Blunt Tip 10 mm with 5 mm Reducer simplifies open laparoscopy.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0124-2015·2014-11-05
Cook Medical Recalls Spirotome Soft-Tissue Biopsy Needle Sets
Cook Medical is voluntarily recalling Spirotome Soft-Tissue Biopsy Needle Sets because protective caps may have dislodged inside the packaging.
Product
Spirotome" Soft-Tissue Biopsy Needle Set. The Spirotome Biopsy Needle Set includes a two-part introducer needle that consists of a cutting cannula and a trocar stylet, a helical-tip biopsy needle that has been sized to fit through the lumen of the cutting cannula. The…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0152-2015·2014-11-05
Elekta Recalls Laksell Gamma Knife Perfexion Units Due to Latch Defect
Elekta is recalling 181 Laksell Gamma Knife Perfexion units because latches may lock before being fully turned, resulting in a poorly locked frame.
Product
Laksell Gamma Knife Perfexion
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0139-2015·2014-11-05
Biosense Webster Recalls ThermoCool SmartTouch Navigation Catheters for Labeling
Biosense Webster is recalling ThermoCool SmartTouch Navigation Catheters to provide additional labeling for safe and effective use.
Product
ThermoCool SmartTouch Navigation Catheters, Catalog No. D132701, D132702, D132703, D132704, D132705, D133601, D133602, D133603.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0134-2015·2014-11-05
Cooper Vision Recalls ProClear Toric Contact Lenses for Axis Defect
Cooper Vision is recalling ProClear Toric contact lenses because routine quality monitoring found that some lots were manufactured with the cylinder axis outside allowable specifications.
Product
ProClear Toric contact lenses are made from a material containing 62% water and 38% omafilcon B, a random copolymer of 2-hydroxyethylmethacrylate and methacrylic acid. The lenses have a tint (VAT Blue 6) which is added to make the lens more visible for handling.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0093-2015·2014-11-05
Martin Avenue Pharmacy Recalls Hydroxocobalamin Injectable Due to Sterility Concerns
Martin Avenue Pharmacy is voluntarily recalling Hydroxocobalamin 10 mg/mL injectable vials due to quality control observations that present a risk to sterility assurance.
Product
Hydroxocobalamin 10 mg/mL injectable packaged in an amber glass injectable vial, Martin Avenue Pharmacy, 1247 Rickert Dr, Naperville, IL.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0126-2015·2014-11-05
Bausch & Lomb Recalls Equate Moisture Last Contact Lens Solution
Bausch & Lomb is recalling Equate Moisture Last Multi-Purpose Solution because the product did not meet disinfectant specifications at the time of manufacture.
Product
Equate Moisture Last Multi-Purpose Solution, 2 pack, 12 fl. oz. (355 mL), Distributed by Walmart Stores, Inc.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0052-2015·2014-11-05
Valeant Recalls APLENZIN Tablets Due to Missing Package Insert
Valeant Pharmaceuticals is recalling APLENZIN extended-release tablets because the package insert is incorrect or missing. Consumers should contact their healthcare provider.
Product
APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 348 mg, a) 7-count HDPE bottle (NDC 0024-5811-07), b) 30-count HDPE bottle (NDC 0024-5811-30), Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0053-2015·2014-11-05
Valeant Recalls APLENZIN Tablets Due to Missing Package Insert
Valeant Pharmaceuticals is recalling APLENZIN (bupropion hydrobromide) extended-release tablets because the package insert is incorrect or missing.
Product
APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 522 mg, a) 7-count HDPE bottle (NDC 0024-5812-07), b) 30-count HDPE bottle (NDC 0024-5812-30), Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0051-2015·2014-11-05
Valeant Recalls APLENZIN Tablets Due to Missing Package Insert
Valeant Pharmaceuticals is recalling 20,499 bottles of APLENZIN (bupropion hydrobromide) 174 mg tablets because the package insert is incorrect or missing.
Product
APLENZIN¿ (bupropion hydrobromide), extended-release tablets, 174 mg, 7-count HDPE bottle, Rx Only, Manufactured by Valeant Pharmaceuticals International, Inc. Steinbach MB, Canada R5G 1Z7, NDC 0024-5810-07.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·14T014000·2014-11-04
Toyo Recalls Tires Due to Tread and Belt Separation Risk
Toyo is recalling specific OPEN Country H/T Tuff Duty and Nitto Dura Grappler tires because stress may cause tread or belt separation, increasing crash risk.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V698000·2014-11-04
Porsche Recalls 2014-2015 Models Due to Hood Latch Defect
Porsche is recalling 2014-2015 911, Boxster, and Cayman vehicles because the front hood latch may fail, potentially opening the hood and blocking the driver's view.
Product
PORSCHE — PORSCHE BOXSTER, CAYMAN, 911
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V700000·2014-11-04
Honda Recalls Multiple Models for Air Bag Inflator Rupture Risk
Honda is recalling specific 2001-2006 models sold in high-humidity areas because the passenger air bag inflator may rupture during deployment.
Product
HONDA — HONDA, ACURA CIVIC HYBRID, PILOT, RIDGELINE, RL
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V699000·2014-11-04
Keystone Recalls 2015 Laredo Trailers Due to Fire Risk
Keystone RV Company is recalling 2015 Laredo trailers because a circuit breaker may rub against the propane cylinder, increasing the risk of fire.
Product
KEYSTONE — KEYSTONE LAREDO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V697000·2014-11-04
Jayco Recalls 2015 Jay Flight Trailers Due to Incorrect Load Labels
Jayco is recalling 2015 Jay Flight trailers because cargo capacity labels may overstate load limits, creating a risk of tire failure and crashes.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V690000·2014-11-03
Airstream Recalls 2014-2015 Travel Trailers Due to Electrical Fire Risk
Airstream is recalling 2014-2015 travel trailers because loose power inlet receptacles may cause excessive heat and vehicle fire.
Product
AIRSTREAM — AIRSTREAM LAND YACHT, FLYING CLOUD, INTERNATIONAL, SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·14V693000·2014-11-03
HME Recalls 2000-2006 1871 Emergency Vehicles for Accelerator Pedal Defect
HME is recalling 2000-2006 1871 emergency vehicles because accelerator pedal springs may break, causing unintended acceleration and increasing crash risk.
Product
HME — HME 1871
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·14V696000·2014-11-03
Jayco Recalls 2015 Eagle Fifth Wheel Trailers for Incorrect Weight Labels
Jayco is recalling 268 model year 2015 Eagle fifth wheel trailers because incorrect weight calculations on the cargo label could lead to overloading and tire failure.
Product
JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL EAGLE
Category
Vehicle
Distribution
Distributed nationwide