State

US Virgin Islands product recalls

73,382 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 73,382 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

20751–20775 of 73559

HighFDA (Devices)·Z-1042-2022·2022-05-18
Medtronic IN.PACT Admiral balloon catheters recalled for damaged packaging
Medtronic is recalling IN.PACT Admiral paclitaxel-coated balloon catheters due to damaged packaging that may result in loss of sterility, affecting approximately 6,035 units worldwide.
Product
Medtronic IN.PACT Admiral, Paclitaxel-coated PTA Balloon Catheter, Sterile EO, Rx Only for the following model Numbers:ADM04004013P ADM04008013P ADM04008013P ADM04008013P ADM04012013P ADM04015013P ADM04015013P ADM04025013P ADM05004013P ADM05004013P ADM05006013P ADM05006013P…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1037-2022·2022-05-18
Surgical Device Kits Recalled Due to Improper Sterilization Process
American Contract Systems is recalling ACS Arthroscopy, Knee, and Hand surgical kits because they were sterilized using a higher than specification ethylene oxide concentration.
Product
1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1046-2022·2022-05-18
Olympus BF-MP60 Bronchofiberscope Recall: Updated Sterilization and Reprocessing Instructions
Olympus is updating instructions for reprocessing and sterilizing BF-MP60 bronchofiberscopes to ensure proper procedures. All 60 units distributed nationwide are affected.
Product
BF-MP60: OES Bronchofiberscope
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0862-2022·2022-05-18
Fagron recalls Nandrolone Decanoate USP for subpotency in multiple lots
Fagron, Inc. is recalling 58 containers of Nandrolone Decanoate USP for prescription compounding due to subpotency. The affected lots were distributed nationwide.
Product
Nandrolone Decanoate, USP, 100 g per plastic container, Rx Only, For Prescription Compounding, Fagron, Inc. 2400 Pilot Knob Rd., St Paul, MN 55120. NDC 51552-1564-04
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1040-2022·2022-05-18
ACS Cath Lab Packs Sterilized with Excess Ethylene Oxide
American Contract Systems recalls ACS Cath Lab Packs distributed in IL, MO, NE, and TX because they were sterilized with higher than specification ethylene oxide concentrations.
Product
ACS Cath Lab Pack
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0865-2022·2022-05-18
Prescription Compounding Drug Nandrolone Decanoate Recalled for Subpotency
Fagron, Inc. is recalling 2 containers of Nandrolone Decanoate USP used for prescription compounding because the product is subpotent, containing less active ingredient than expected. The recall is nationwide.
Product
Nandrolone Decanoate, USP, 500 g per plastic container, Rx Only, For Prescription Compounding, Distributed by: Humco, 7400 Alumax Road, Texarkana, TX 75501. NDC 0395-8212-56
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0857-2022·2022-05-18
Bupropion Hydrochloride 150 mg Extended-Release Tablets Recalled for Activated Carbon Contamination
Sun Pharmaceutical is recalling Bupropion Hydrochloride 150 mg extended-release tablets distributed nationwide due to activated carbon particles from desiccant canisters found in bottles. No illnesses have been reported.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0863-2022·2022-05-18
FDA recalls Nandrolone Decanoate compounding ingredient for subpotency nationwide
Fagron, Inc. recalls 53 containers of Nandrolone Decanoate compounding ingredient due to subpotency. The product was distributed nationwide.
Product
Nandrolone Decanoate, USP, 500 g per plastic container, Rx Only, For Prescription Compounding, Fagron, Inc. 2400 Pilot Knob Rd., St Paul, MN 55120. NDC 51552-1564-05
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0866-2022·2022-05-18
FDA Recalls Subpotent Nandrolone Decanoate Compounding Ingredient
Fagron, Inc initiated a nationwide recall of Nandrolone Decanoate compounding ingredient due to subpotency. The affected lot may contain below-strength concentrations of the active pharmaceutical ingredient.
Product
Nandrolone Decanoate, USP, 1 kg per plastic container, Rx Only, For Prescription Compounding, Distributed by: Humco, 7400 Alumax Road, Texarkana, TX 75501. NDC 0395-8212-43
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0864-2022·2022-05-18
FDA Recalls Subpotent Nandrolone Decanoate Compounding Ingredient from Fagron
Fagron Inc. initiated a voluntary recall of 68 containers of Nandrolone Decanoate USP in March 2022 after the product was found subpotent, containing less active ingredient than labeled. The recall affects compounding pharmacies nationwide.
Product
Nandrolone Decanoate, USP, 1 kg per plastic container, Rx Only, For Prescription Compounding, Fagron, Inc. 2400 Pilot Knob Rd., St Paul, MN 55120. NDC 51552-1564-07
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0858-2022·2022-05-18
Bupropion Extended-Release Tablets Recalled for Activated Carbon Contamination
Sun Pharmaceutical is recalling Bupropion Extended-Release 200mg tablets after customers found activated carbon particles inside bottles from the desiccant canister.
Product
BUPROPION HYDROCHLORIDE — BUPROPION HYDROCHLORIDE (BUPROPION HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0861-2022·2022-05-18
Esomeprazole Magnesium Delayed-Release Capsules Recalled for Failed Quality Specifications
Mylan Institutional is recalling Esomeprazole Magnesium Delayed-Release Capsules 40 mg due to failed impurity specifications found during stability testing, affecting 885 cartons nationwide.
Product
Esomeprazole Magnesium Delayed-Release Capsules, USP 40 mg, packaged in Unit Dose Blister Cards of 6 (10 cards of 6 Capsules each per carton), Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 USA. NDC 42292-010-16
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-1056-2022·2022-05-18
Bone Graft Syringe Recall: Patient Chart Labels List Incorrect Part Numbers
Cerapedics is recalling putty i-FACTOR Peptide Enhanced Bone Graft syringes because patient chart labels contain incorrect Part Numbers and volume amounts. The company discovered the labeling discrepancy in 572 units distributed nationwide.
Product
putty i-FACTOR Peptide Enhanced Bone Graft 1.0cc Syringe REF 700-010, PUTTY
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·22V345000·2022-05-17
Vanguard VIP-53 Trailers Recalled for Insufficient Wheel Hub Lubrication
Vanguard is recalling two 2022 VIP-53 trailers because insufficient wheel hub lubrication could cause bearing failure and loss of control.
Product
VANGUARD — VANGUARD VIP-53
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V346000·2022-05-17
2021 Ford Expedition and Navigator: Engine Compartment Fire Risk Recall
Ford is recalling certain 2021 Expedition and Lincoln Navigator vehicles due to risk of engine compartment fire while driving or parked. Owners should park vehicles outside away from structures until repairs are available.
Product
FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V343000·2022-05-17
2020-2023 Trailstar and Ranger Trail Boat Trailers Recalled for Hub Seizure
Tracker Marine is recalling 2020-2023 Trailstar and Ranger Trail boat trailers because axle hubs were not tightened properly, which can cause hub seizure and loss of vehicle control.
Product
TRAILSTAR — TRAILSTAR, RANGER TRAIL BOAT TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V344000·2022-05-17
2022 Kia Telluride recall: instrument cluster display may go blank
Excess adhesive in the instrument cluster circuit board may cause the display to go blank, preventing drivers from seeing critical information and increasing crash risk.
Product
KIA — KIA TELLURIDE
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V340000·2022-05-16
FCCC MT50E Vans Recalled for Shift Knob Malfunction
Daimler Trucks North America is recalling 2021-2022 FCCC MT50E walk-in vans because a faulty shift knob may cause unintended movement.
Product
FCCC — FCCC MT50E
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22E039000·2022-05-16
Carparts.com Recalls Oil Filter Housings Due to Leak and Fire Risk
Carparts.com is recalling specific oil filter housings because a seal defect may cause oil leaks, increasing the risk of fire or engine failure.
Product
ENGINE AND ENGINE COOLING:ENGINE:OIL/LUBRICATION:FILTER/SCREEN recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V339000·2022-05-16
2022 Freightliner Cascadia trucks recalled for disabled antilock brakes and stability control
Daimler Trucks North America is recalling approximately 17 certain 2022 Freightliner Cascadia trucks because the antilock brakes and electronic stability control can be manually disabled, violating federal safety standards and increasing crash risk. The company will repurchase affected vehicles.
Product
FREIGHTLINER — FREIGHTLINER CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V338000·2022-05-16
Commercial trucks recalled for incorrect gross axle weight labels
Daimler Trucks is recalling commercial trucks with incorrect weight-rating labels that could allow unsafe overloading. Dealers will replace the labels free of charge.
Product
WESTERN STAR — WESTERN STAR, FREIGHTLINER 4900, 4700, 5700, NEW CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V342000·2022-05-16
Bowlus Endless Highways Travel Trailers Recalled for Gas Leak Risk
Bowlus is recalling 2022 Endless Highways travel trailers because damaged burner control valves may cause a gas leak, increasing fire risk.
Product
BOWLUS — BOWLUS ENDLESS HIGHWAYS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V341000·2022-05-16
Utilimaster Walk-in Van Recall for Incorrect Tire Placard Information
Shyft Group is recalling 2022 Utilimaster Walk-in vans because tire size and pressure labels may be incorrect, potentially leading to improper tire inflation.
Product
UTILIMASTER — UTILIMASTER WALK-IN VAN
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V333000·2022-05-13
Ford Recalls 2021 Mustang Mach-E Vehicles for Software Defect
Ford is recalling 2021 Mustang Mach-E all-wheel drive vehicles because a software error may cause unintended acceleration or loss of power.
Product
FORD — FORD MUSTANG MACH E
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V337000·2022-05-13
Ford Recalls 2016 Super Duty Trucks for Air Bag Defect
Ford is recalling 2016 Super Duty trucks because dust in the steering wheel clock spring may prevent the driver's air bag from deploying.
Product
FORD — FORD F-350 SD, F-550 SD, F-450 SD, F-250 SD
Category
Vehicle
Distribution
Distributed nationwide