State

US Virgin Islands product recalls

73,388 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: 2026-09-23

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 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21201–21225 of 73565

HighFDA (Devices)·Z-0848-2022·2022-04-06
Radiation therapy planning software subject to jaw positioning errors during optimization
RayStation radiation therapy planning software (versions 6-11A) may unexpectedly change jaw positions during optimization after dose or target modifications. Users should verify treatment plans carefully before delivery.
Product
TomoHelical and TomoDirect plans in RayStation 6, 7, 8A, 8B, 9A, 9B, 10A, 10B and 11A. Build Numbers: 6.1.1.2, 6.2.0.7, 6.3.0.6, 7.0.0.19, 8.0.0.61, 8.0.1.10, 8.1.0.47, 8.1.1.8, 8.1.2.5, 9.0.0.113, 9.1.0.933, 9.2.0.483, 10.0.0.1154, 10.0.1.52, 10.1.0.613, 11.0.0.951 or…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0737-2022·2022-04-06
Lansoprazole Capsules Recalled for Failed Dissolution in Stability Testing
Dr. Reddy's Laboratories is recalling specific lots of Lansoprazole 15 mg delayed-release capsules nationwide because the capsules failed to dissolve properly during long-term stability testing, which could affect medication effectiveness.
Product
LANSOPRAZOLE — LANSOPRAZOLE (LANSOPRAZOLE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0734-2022·2022-04-06
Testosterone Cypionate Injectable Vials Recalled for Lack of Sterility Assurance
Drug Depot, Inc. is recalling 24 vials of Testosterone Cypionate 200 MG/ML Injectable nationwide due to lack of sterility assurance. The product was distributed throughout the USA and Puerto Rico.
Product
TESTOSTERONE CYPIONATE *GS* Oil 200 MG/ML Injectable, Packaged in a multi dose 10ML vial, Formula ID 76681, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0850-2022·2022-04-06
Medical software recall: RayStation radiation therapy dose calculation errors
RayStation and RayPlan radiation therapy planning software may calculate incorrect radiation doses due to a source-to-skin distance calculation error. The FDA Class II recall affects 149 units distributed in the US.
Product
RayStation 4-11B, and RayPlan 1, 2, 7-11B including some service packs: RayStation 4.0 (4.0.0.14) to RayStation 5 Service Pack 2 (5.0.2.35), RayStation 5 Service Pack 3 (5.0.3.17), RayStation 6/RayPlan 2 (6.0.0.24), RayStation 6/RayPlan 2 Service Pack 1 (6.1.1.2)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0852-2022·2022-04-06
Hanger-Bar 2P 45cm Recalled for Fall Hazard from Loosened Set Screw
Human Care USA, Inc. is recalling the Hanger-Bar 2P 45cm because the set screw may loosen due to a manufacturing defect, creating a fall hazard.
Product
Hanger-Bar 2P 45cm
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0829-2022·2022-04-06
Liko Universal Twinbar 670 QRH Patient Lift Accessory Recalled for Fall Risk
Baxter Healthcare Corporation is recalling 1,399 Liko Universal Twinbar 670 QRH patient lift accessories due to an incorrect center bolt used during assembly. The defect could cause a patient to fall during use.
Product
Liko Universal Twinbar 670 QRH, an accessory that can be used together with most Liko lifts, model numbers 3156087 and P3156087.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0730-2022·2022-04-06
Injectable testosterone-anastrozole mixture recalled for sterility assurance failure
Drug Depot (APS Pharmacy) is recalling testosterone cypionate/anastrozole injectable oil due to lack of sterility assurance. The recall affects 846 vials distributed nationwide.
Product
TESTOSTERONE CYPIONATE/ANASTROZOLE *GS* OIL 200MG/1MG/ML Injectable, Packaged in a multi dose 10ML vial, as a) 4 ML Formula ID 115387; b) (RM) 10 ML Formula ID 115125; APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0729-2022·2022-04-06
Gonadorelin injectable recalled for lack of sterility assurance
Drug Depot recalls 1,843 vials of Gonadorelin injectable nationwide due to lack of sterility assurance. Patients should consult their healthcare provider regarding previously dispensed doses.
Product
(CA) GONADORELIN (4ML) 0.2 MG/ML INJECTABLE, Packaged in a multi dose 10ML vial, Formula ID136345, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0733-2022·2022-04-06
Injectable Testosterone Recalled Due to Lack of Sterility Assurance
Drug Depot's testosterone injection product was recalled nationwide for lack of sterility assurance. Affected consumers should discontinue use and consult their healthcare provider.
Product
TESTOSTERONE CYPIONATE/PROPIONATE *SES* Oil (10 ML) 160MG/20MG/ML Injectable, Packaged in a multi dose 10ml vial, Formula ID 115498, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·22V223000·2022-04-06
Arcimoto Motorcycles Charging System Disabled at Freezing Temperatures
Arcimoto is recalling 2019-2022 FUV, Rapid Responder, Deliverator, and Roadster motorcycles. The charging system may disable at freezing temperatures, potentially causing unexpected stalls and increasing crash risk.
Product
ARCIMOTO — ARCIMOTO FUV, DELIVERATOR, RAPID RESPONDER, ROADSTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0836-2022·2022-04-06
Revogene diagnostic device recalled for photomultiplier tube malfunction
Meridian Bioscience is recalling Revogene diagnostic devices due to compromised photomultiplier tubes that may produce false-positive or indeterminate test results.
Product
Revogene, For In Vitro Diagnostic use in performing nucleic acid testing in clinical laboratories. Meridian branded Revogene: Catalog Number 610210 GenePOC branded Revogene: Catalog Number 130840
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0909-2022·2022-04-06
Schwan's Spinach & Artichoke Dip recalled due to product mislabeling
Fairmont Foods is recalling Schwan's Spinach & Artichoke Dip because cartons may contain Chicken & Broccoli instead, creating potential allergen risks.
Product
Schwan's Spinach & Artichoke Dip. Item Number 061353, UPC 10038-68192. Net Wt. 24 oz. (1 lb. 8 oz.) 680g. Contains: 2 Bowls. Keep Frozen. Cook Thoroughly. Spinach and Artichokes blended with cream cheese and sour cream with Parmesan, Mozzarella, and Romano Cheeses.…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0832-2022·2022-04-06
Ambulatory infusion pumps recalled due to erroneous software installation
InfuTronix is recalling Nimbus PainPro ambulatory infusion pumps after an unreleased software version was installed in error. The defective units may impact patient safety.
Product
Nimbus PainPro Ambulatory Infusion Pumps with software version v4, Model Number IT1072, sold as kit IT1075-DUKE-HSP, IT1076-DUKE-HSP and IT1077-DUKE-HSP
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V221000·2022-04-06
Prevost Recalls 2010-2023 Buses Due to Alternator Belt Fire Risk
Prevost is recalling 6,342 buses from 2010-2023 because a seizing alternator bearing can overheat and cause a fire. Owners will receive free belt replacements.
Product
PREVOST — PREVOST H3-45, H3-45 VIP, X3-45, X3-45 COMMUTER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0851-2022·2022-04-06
Hanger-Bar 2P Medical Device Recalled for Loosening Set Screw
Human Care USA, Inc. is recalling the Hanger-Bar 2P 45cm due to a manufacturing defect allowing the set screw to loosen, creating a fall hazard.
Product
Hanger-Bar 2P 45cm
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22E031000·2022-04-06
Volkswagen Recalls Rear Hatch Spoilers for 2018-2022 Tiguan Vehicles
Volkswagen is recalling rear hatch spoilers for 2018-2022 Tiguan long wheel base vehicles because incorrect installation instructions may cause the spoiler to detach.
Product
STRUCTURE:BODY recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0855-2022·2022-04-06
Medtronic MiniMed insulin pumps may not deliver basal insulin without configuration
Medtronic MiniMed insulin pumps may be used without programmed basal rates, causing insulin under-delivery and potentially severe high blood sugar. Patients must configure and save basal settings before use, but labeling doesn't clearly explain this requirement.
Product
MiniMed 630G: MMT-1715, MMT-1754, MMT-1755; MiniMed 670G: MMT-1740, MMT-1741, MMT-1742, MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782; MiniMed 770G: MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892; MiniMed 620G (OUS Only): MMT-1750; MiniMed 640G (OUS…
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-0849-2022·2022-04-06
Radiation therapy planning software: incorrect dose density calculation
RayStation/RayPlan radiation therapy software (versions 4–11A) may incorrectly calculate radiation dose density in treatment planning. The error affects dose calculations in regions partially covered by certain structures.
Product
RayStation/RayPlan versions 4 - 11A, including service packs. Build Stations: 4.0.0.14, 4.0.3.4, 4.3.0.14, 4.5.1.14, 4.7.2.5, 4.7.3.13, 4.7.4.4, 4.7.5.4, 4.7.6.7, 4.9.0.42, 5.0.1.11, 5.0.2.35, 5.0.3.17, 6.0.0.24, 6.1.1.2, 6.2.0.7, 6.3.0.6, 7.0.0.19, 8.0.0.61, 8.0.1.10…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0731-2022·2022-04-06
Testosterone Cypionate/Anastrozole Injectable Recalled for Sterility Assurance Defect
APS Pharmacy is recalling 73 vials of Testosterone Cypionate/Anastrozole oil due to lack of sterility assurance. The product was distributed nationwide including Puerto Rico.
Product
TESTOSTERONE CYPIONATE/ ANASTROZOLE *GS* OIL (10ML) 200MG/0.5MG/ML; Packaged in a multi dose 10ML vial, as a) (CA) 4 ML Formula ID 136164; b) (RM) 10 ML Formula ID 115962; APS Phar
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0843-2022·2022-04-06
Hip prosthetic femoral head component size and offset labeling mismatch
Howmedica Osteonics is recalling 40 units of Biolox delta Ceramic V40 Femoral Head components where the size and/or offset may not match package labeling.
Product
Biolox delta Ceramic V40 Femoral Head 32/ +4.0mm Catalog Number: 6570-0-232
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V226000·2022-04-06
2022 Volkswagen Tiguan rear spoiler risks detaching from vehicle
2022 Volkswagen Tiguan vehicles are recalled due to insufficient attachment of the rear hatch spoiler. The spoiler may separate from the vehicle, creating a road hazard and increasing crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN TIGUAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V222000·2022-04-06
Volvo Bus Recalls 2020 9700 DOT Vehicles Due to Fire Risk
Volvo Bus is recalling 48 2020 9700 DOT vehicles because a seizing alternator bearing can overheat and cause a fire. Owners will receive replacement belts free of charge.
Product
VOLVO BUS — VOLVO BUS 9700
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0735-2022·2022-04-06
Testosterone Cypionate Injectable Recalled for Lack of Sterility Assurance
Drug Depot recalled 17 vials of Testosterone Cypionate Injectable due to lack of sterility assurance in manufacturing. The recalled product was distributed nationwide and should not be used.
Product
TESTOSTERONE CYPIONATE *GS* (2 mL) 80 MG/ML Injectable, Packaged in a multi dose 10ML vial, Formula ID 127492, APS Pharmacy
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0830-2022·2022-04-06
Siemens Magnesium Flex reagent cartridge recalled for imprecision and assay errors
Siemens recalls magnesium reagent cartridges due to imprecision and abnormal assay flags that may cause erroneous diagnostic results and require repeat patient testing.
Product
Siemens Dimension Vista Magnesium Flex reagent cartridge (MG) Material # 10445158, Catalog # K3057 used in the Dimension Vista System. The Dimension Vista Magnesium Flex Reagent (MG) method is an In vitro diagnostic test for the quantitative measurement of magnesium in…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0847-2022·2022-04-06
BALLARD Multi-Access Port Catheter Recalled for Incorrect Expiration Date
Avanos Medical is recalling 2,520 BALLARD Multi-Access Port Catheters due to incorrect expiration dates on the packaging. No illnesses or injuries have been reported. Patients should verify the lot number and contact their healthcare provider.
Product
BALLARD* Multi-Access Port (MAP) Catheter, Double Swivel Y- Adult, 16 French; Sterile; Single Use
Category
Medical Device
Distribution
Distributed nationwide