State

US Virgin Islands product recalls

73,478 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total: 177
Critical: 12
Severe: 39
Most recent: 2026-10-14

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22826–22850 of 73655

SevereCPSC·22021·2021-11-18
Goodman evaporator coil drain pans recalled for fire hazard
Goodman Manufacturing is recalling evaporator coil drain pans used in residential gas furnaces because the plastic drain pan can overheat, melt, and deform, posing a fire hazard. The company has received 23 reports of fire incidents involving the drain pans, resulting in significant fire and smoke damage to residences.
Product
Evaporator coil drain pans installed with residential condensing gas furnaces in an up-flow configuration
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·21V901000·2021-11-18
Honda Recalls 2021 NC750XD Motorcycles for Fuel Injection Software Defect
Honda is recalling 2021 NC750XD motorcycles because incorrect fuel injection software may cause stalling, increasing crash risk.
Product
HONDA — HONDA NC750XD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V900000·2021-11-18
2021 Honda Accord automatic seat belt retractor may fail to lock
Honda is recalling certain 2021 Accord and other model vehicles because the automatic locking retractor on the second-row center seat belt may deactivate improperly, potentially leaving child restraints unsecured in a crash.
Product
HONDA — HONDA CR-V HYBRID, ACCORD HYBRID, RIDGELINE, ACCORD
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V897000·2021-11-18
Jayco Recalls 2021 Jay Flight Octane Travel Trailers Due to Water Heater Defect
Jayco is recalling 2021 Jay Flight Octane travel trailers because the water heater was installed in the wrong location, which could allow exhaust fumes to enter the trailer.
Product
JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT OCTANE
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22020·2021-11-18
Honda Pioneer and Talon Recreational Vehicles Steering Loss Recall
American Honda is recalling about 1,400 Honda Pioneer 700, Pioneer 1000, and Talon 1000 recreational off-highway vehicles equipped with electric power steering. The vehicles can lose steering function, posing crash and injury hazards.
Product
Honda Pioneer and Talon ROVs
Category
Vehicle
Distribution
Distributed nationwide
ModerateCPSC·22711·2021-11-18
AmazonBasics Memory Foam Mattresses Recalled for Fire Hazard
Amazon is recalling about 15,300 AmazonBasics Memory Foam Mattresses sold between April 2020 and March 2021 because they fail to meet federal flammability standards, posing a fire hazard. No injuries have been reported.
Product
AmazonBasics Memory Foam Mattresses
Category
Consumer Product
Distribution
Distributed nationwide
SevereNHTSA·21V890000·2021-11-17
Toyota Recalls 2018-2019 Camry Vehicles for Vacuum Pump Defect
Toyota is recalling 2018-2019 Camry vehicles because a vacuum pump component may break, causing a sudden loss of braking assist and increasing crash risk.
Product
TOYOTA — TOYOTA CAMRY
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V891000·2021-11-17
Sutphen Recalls 2020 Fire Trucks Due to Power Steering Pump Defect
Sutphen is recalling 2020 Fire trucks because pressure in the power steering pump may break the shaft seal, causing a loss of steering assist and increasing crash risk.
Product
SUTPHEN — SUTPHEN FIRE TRUCK
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V892000·2021-11-17
2021 Volkswagen Atlas and 2020-2021 Cross Sport recalled for air bag water damage
Volkswagen is recalling certain 2021 Atlas and 2020-2021 Cross Sport vehicles whose air conditioning drain tube can become blocked, allowing water to damage the air bag control module and potentially trigger inadvertent air bag deployment.
Product
VOLKSWAGEN — VOLKSWAGEN ATLAS, ATLAS CROSS SPORT
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0169-2022·2021-11-17
Bobo's Almond Butter Protein Bars recalled for undeclared peanuts
Simply Delicious, Inc. is recalling Bobo's Almond Butter Protein Bars (2.2 oz.) because they contain undeclared peanuts, posing a risk to consumers with peanut allergies.
Product
Bobo's Almond Butter Protein Bar, 2.2 oz., 4-pack Multipack, Master Case with 6 sleeves. UPC 8-29262-00201-6 (Individual bar) UPC 8-29262-00326-6 (4-Pack Multipack) UPC 8-29262-00370-9 (Master Case of 6 sleeves) Storage ambient.
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·21V893000·2021-11-17
Motorhome seat belt retractor defect affects child restraint systems
Jayco recalls certain 2021-2022 motorhomes with defective seat belt retractors that may fail to secure child restraint systems during crashes. Dealers will replace the retractors free of charge.
Product
JAYCO — JAYCO, ENTEGRA SWIFT, ETHOS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0208-2022·2021-11-17
Safety Blood Collection Needle Recalled for Safety Mechanism Activation Issues
Zhejiang Kindly Medical Devices is recalling Henry Schein Safety Blood Collection Needles due to potential difficulty activating the safety mechanism. Affected lot numbers distributed nationwide.
Product
HENRY SCHEIN Safety Blood Collection Needle 21Gx 1 1/4 Inch, REF 570-2067, 100pcs/box 1000pcs/ctn 350*210*350mm
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V896000·2021-11-17
Freightliner and Western Star trucks recalled for unapproved tires and wheels
Daimler Trucks North America is recalling Freightliner 108SD, 114SD, Coronado, and Western Star trucks from model years 2012-2022 due to unapproved tires and rims that do not meet federal safety standards.
Product
WESTERN STAR — WESTERN STAR, FREIGHTLINER 49X, 4900, 4700, 114SD
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0207-2022·2021-11-17
McKesson PREVENT HT Winged Blood Collection Needles Recall for Safety Mechanism Difficulty
McKesson PREVENT HT Safety Winged Blood Collection Needles may have difficulty activating their safety mechanism. The recall affects units distributed nationwide.
Product
McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH21GS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0211-2022·2021-11-17
QuikClot Combat Gauze Recalled for Potential Sterile Packaging Seal Failure
Z-Medica is recalling 2400 units of QuikClot Combat Gauze due to potential packaging seal failures that could compromise sterile barrier integrity. Affected lot 12645 was distributed nationwide.
Product
QuikClot Combat Gauze-For Temporary External Use To Control Traumatic Bleeding Model / Part# 200
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0213-2022·2021-11-17
Philips Azurion X-Ray Systems may lock up during simultaneous button presses
Philips Azurion Interventional X-Ray Systems (software 2.1.x) may experience imaging lock-up when operators simultaneously press both the APC and Float Tabletop buttons.
Product
Philips Azurion Interventional Fluoroscopic X-Ray System, Software version 2.1.x, Model numbers 722063, 722064, 722067, 722068, 722078, 722079, 722221, 722222, 722223, 722224, 722225, 722226, 722227, 722228. (Azurion 3 M12, Azurion 3 M15, Azurion 5 M12, Azurion 5 M20, Azurion 7…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0205-2022·2021-11-17
McKesson Safety Blood Collection Needles Recalled Over Safety Mechanism Activation Risk
Nationwide recall of McKesson PREVENT HT Safety Blood Collection Needles (22G 1 1/4 inch) due to potential difficulty activating the safety mechanism. The protective feature may fail to engage properly during use.
Product
McKesson PREVENT HT Safety Blood Collection Needles, 22G 1 1/4 inch, MFR # 16-NBC22GS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0204-2022·2021-11-17
McKesson Safety Blood Collection Needles Recalled for Safety Mechanism Defect
McKesson PREVENT HT Safety Blood Collection Needles are being recalled due to potential difficulty in activating the safety mechanism. The recall affects needles distributed nationwide, including specific lot numbers with expiration dates through May 2025.
Product
McKesson PREVENT HT Safety Blood Collection Needles, 21G 1 1/4 inch, MFR # 16-NBC21GS
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V889000·2021-11-17
Toyota Recalls 2022 Sienna Models Due to Seat Belt Webbing Guide Defect
Toyota is recalling 2022 Sienna and Sienna Hybrid vehicles with eight-passenger seating because an incorrect seat belt webbing guide may cause the belt to tear during a crash.
Product
TOYOTA — TOYOTA redundant SIENNA, SIENNA HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0206-2022·2021-11-17
McKesson PREVENT HT Blood Collection Needle Safety Mechanism Activation Issue
McKesson PREVENT HT blood collection needles with specific lot numbers may have difficulty activating their safety mechanism. Healthcare facilities should contact the manufacturer for replacement guidance.
Product
McKesson PREVENT HT Safety Winged Blood Collection Needle with Tube Holder, MFR # 16-NBCH22GS
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0215-2022·2021-11-17
Hemodialysis Delivery System Software May Use Incorrect Treatment Parameters
Baxter's Hemodialysis Delivery System may incorrectly revert to old prescription values when operators change prescriptions after filter changes, potentially resulting in incorrect treatment parameters.
Product
Hemodialysis Delivery System, Software Version 2.x.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0209-2022·2021-11-17
Safety Blood Collection Needles Recalled Due to Safety Mechanism Activation Difficulty
Henry Schein safety blood collection needles may have difficulty activating their safety mechanism, potentially increasing needlestick injury risk. Affected lots were distributed nationwide with expiration dates through late 2025.
Product
HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0229-2022·2021-11-17
Cefixime Capsules 400 mg Recalled for Failed Impurities and Degradation Specifications
Ascend Laboratories LLC is recalling Cefixime Capsules 400 mg nationwide due to failed impurities and degradation specifications. The affected lot is Lot 20140282 with an expiration date of December 2021.
Product
CEFIXIME — CEFIXIME (CEFIXIME)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0231-2022·2021-11-17
Tadalafil Tablets Recalled Due to Incorrect Product Formulation
Sun Pharmaceutical is recalling Tadalafil Tablets USP 20 mg due to use of an incorrect grade of Crospovidone during manufacturing. The recall affects 36,786 bottles distributed to one distributor.
Product
TADALAFIL — TADALAFIL (TADALAFIL)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0230-2022·2021-11-17
Tadalafil Tablets Recalled for Incorrect Product Formulation
Sun Pharmaceutical Industries is recalling Tadalafil 5 mg tablets (Lot # DNC1127A) because an incorrect grade of Crospovidone was used during manufacturing. The product was distributed to one distributor who may have further distributed it nationwide.
Product
TADALAFIL — TADALAFIL (TADALAFIL)
Category
Drug
Distribution
Distributed nationwide