State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41851–41875 of 73919

ModerateFDA (Drugs)·D-1041-2017·2017-08-09
Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.
Product
Divalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054, NDC 68382-031-01
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1043-2017·2017-08-09
Zydus Recalls Divalproex Sodium Tablets for Failed Dissolution Specifications
Zydus Pharmaceuticals is recalling Divalproex Sodium Delayed Release Tablets because they failed to meet dissolution specifications.
Product
Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1057-2017·2017-08-09
PD-Rx Pharmaceuticals Recalls Famotidine 20 mg Tablets for Weight Issues
PD-Rx Pharmaceuticals is recalling 100 bottles of Famotidine USP 20 mg tablets because they failed to meet tablet weight specifications.
Product
Famotidine USP 20 mg, 30 tablets bottle, Rx, PKG By; PD Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 --- NDC 55289-765-30
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1044-2017·2017-08-09
Bayer Recalls Alka-Seltzer Tablets Due to Defective Blister Pack Foil
Bayer HealthCare is recalling Alka-Seltzer Original effervescent tablets because customer complaints confirmed small holes or cracks in the foil of the blister packs.
Product
Alka-Seltzer Original ( 325 mg Aspirin (NSAID), 1916 mg Analgesic, Sodium bicarbonate/Antacid, 1000 mg Anhydrous Citric Acid) Effervescent Tablets, 12-count carton, Made in Germany, Distributed by Bayer HealthCare, LLC Whippany, NJ 07981, UPC 016500040194
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1039-2017·2017-08-09
Teva Recalls Albuterol Sulfate Inhalation Solution Due to Impurities
Teva Pharmaceuticals USA is recalling Albuterol Sulfate Inhalation Solution because high levels of a related compound were detected.
Product
Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials For Inhalation per carton, Rx only, Mfd. for: Watson Laboratories, Inc., Corona, CA 92880; Mfd. by: Cipla Ltd., Verna, Goa INDIA, NDC 0591-3467-53.
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·17V495000·2017-08-08
BMW Recalls 2012-2013 X3 and M6 Models for Air Bag Defect
BMW is recalling 2012-2013 X3 and 2013 M6 vehicles because a defective driver's air bag inflator could cause metal fragments to strike occupants in a crash.
Product
BMW — BMW X3, M6
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V496000·2017-08-08
Dodge Charger and Challenger Recall for Engine Oil Cooler Hose Failure
Chrysler is recalling 2017 Dodge Charger and Challenger vehicles with Hellcat engines because engine oil cooler hoses may fail, causing rapid oil loss and increased crash or fire risk.
Product
DODGE — DODGE CHARGER, CHALLENGER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17E045000·2017-08-08
Hickory Springs Recalls CE White Convertible School Bus Seats
Hickory Springs is recalling CE White Convertible School Bus Seats due to inadequate padding on D-ring mounting studs, which may increase injury risk in rear-end collisions.
Product
SEATS recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17203·2017-08-08
Polaris Recalls Scrambler All-Terrain Vehicles Due to Throttle Switch Failure
Polaris is recalling 2,800 Scrambler XP 1000 ATVs because the throttle release switch can fail, posing a crash hazard. Consumers should stop using the vehicles and contact Polaris for a free repair.
Product
Polaris Scrambler all-terrain vehicle (ATVs)
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17201·2017-08-08
NVIDIA Recalls European Plug Heads for Power Adaptors Due to Shock Hazard
NVIDIA is recalling European plug heads for SHIELD power adaptors because they can break and expose metal prongs, posing an electric shock hazard.
Product
European plug heads for NVIDIA SHIELD™ power adaptors
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17202·2017-08-08
Meijer Recalls Wave Zone Children's Swimsuits Due to Choking Hazard
Meijer is recalling about 22,200 Wave Zone children's swimsuits because snaps can detach, posing a choking hazard to infants and toddlers.
Product
Wave Zone children's swimsuits
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V492000·2017-08-07
Spartan Recalls 2014-2017 Utilimaster Walk-In Vans for Seat Belt Defect
Spartan Motors is recalling 2014-2017 Utilimaster Walk-In Vans because seat belt D-ring mountings may detach in a crash, increasing injury risk.
Product
UTILIMASTER — UTILIMASTER WALK-IN VAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V493000·2017-08-07
Hino Recalls 2018 NV8J, NJ8J, and NE8J Trucks for Door Hinge Bolts
Hino is recalling 2018 NV8J, NJ8J, and NE8J trucks because door hinge bolts may be loose, allowing doors to open while driving.
Product
HINO — HINO NV8J, NJ8J, NE8J
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17E044000·2017-08-07
K&N Recalls Powersports Oil Filters for Leak Risk
K&N Engineering is recalling specific Powersports Oil Filters that may leak oil onto the rear tire or brake, increasing crash risk.
Product
ENGINE AND ENGINE COOLING:ENGINE recall
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17761·2017-08-07
Firewood Recalls Vaporizers Due to Fire Hazard
Firewood is recalling about 400 Firewood 4 vaporizers because an electrical short can cause the battery to catch fire. No injuries have been reported.
Product
Vaporizers
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·17V490000·2017-08-04
Land Rover Recalls One 2017 Range Rover for Fuel Pump Bolt Defect
Jaguar Land Rover is recalling one 2017 Range Rover because a fuel pump bolt may be too long, risking a fuel leak and fire.
Product
LAND ROVER — LAND ROVER RANGE ROVER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V491000·2017-08-04
Jaguar Recalls One 2017 F-PACE for Fuel Pump Bolt Defect
Jaguar is recalling one 2017 F-PACE because a fuel pump bolt may be too long, causing a fuel leak that increases fire risk.
Product
JAGUAR — JAGUAR F-PACE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V494000·2017-08-04
Trail King Recalls 2012-2014 Gooseneck Trailers Due to Pivot Plate Defect
Trail King is recalling 2012-2014 gooseneck trailers because a short pivot plate reinforcement may crack, causing the trailer deck to disconnect and increasing crash risk.
Product
TRAIL KING — TRAIL KING GOOSENECK TRAILER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·17V489000·2017-08-03
McElrath Trailers Recalls 2015-2017 VX30-800 and VX50-800 Models for Frame Defect
McElrath Trailers is recalling 2015-2017 VX30-800 and VX50-800 trailers because the frame may deform, potentially causing the trailer neck to separate from the rear.
Product
MCELRATH TRAILERS — MCELRATH TRAILERS VX30-800, VX50-800
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V487000·2017-08-03
GM Recalls 2017 Silverado and Sierra Trucks for Missing Child Seat Instructions
General Motors is recalling 2017 Chevrolet Silverado 1500 and GMC Sierra 1500 trucks because the owner's manual may lack instructions for child restraint anchorage systems.
Product
CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·17V488000·2017-08-03
BMW Recalls 2014-2017 R1200RT Police Motorcycles for Brake Light Software Issue
BMW is recalling 2014-2017 R1200RT Police motorcycles because brake lights may not illuminate in special operating mode, increasing crash risk.
Product
BMW — BMW R1200 RT POLICE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·17199·2017-08-03
RH Recalls Smythson Shagreen Furniture Due to Sharp Metal Trim Hazards
Restoration Hardware is recalling Smythson Shagreen furniture because metal trim can detach, creating sharp points that pose injury and laceration risks.
Product
Furniture
Category
Consumer Product
Distribution
Distributed nationwide
HighCPSC·17200·2017-08-03
Richie House Children's Robes Recalled for Flammability Violation
Richie House children's robes are being recalled because they fail federal flammability standards, posing a risk of burn injuries to children.
Product
Children's robes
Category
Consumer Product
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2736-2017·2017-08-02
Maquet CS 100i Intra-Aortic Balloon Pump Recalled Due to Device Failure
Maquet Datascope is recalling 12,319 CS 100i Intra-Aortic Balloon Pumps because electrical failures prevented the device from initiating therapy, which has been associated with a patient death.
Product
CS 100i Intra-Aortic Balloon Pump
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2737-2017·2017-08-02
Maquet CS 100 Intra-Aortic Balloon Pump Recalled Due to Device Failure
Maquet Datascope is recalling 12,319 CS 100 Intra-Aortic Balloon Pumps because electrical and autofill failures prevented the device from initiating therapy, which has been associated with a patient death.
Product
CS 100 Intra-Aortic Balloon Pump
Category
Medical Device
Distribution
Distributed nationwide