State

US Virgin Islands product recalls

73,584 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 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27951–27975 of 73762

HighFDA (Devices)·Z-2799-2020·2020-08-19
United Imaging Recalls uEXPLORER PET/CT System for Potential Sharp Edges
Shanghai United Imaging Healthcare is recalling one uEXPLORER PET/CT Diagnostic Imaging System in Texas due to potential sharp edges and image data issues.
Product
uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning and treatment response evaluation for diseases and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2800-2020·2020-08-19
United Imaging Recalls uMI 550 PET/CT Systems Due to Imaging and Safety Defects
Shanghai United Imaging Healthcare is recalling four uMI 550 PET/CT systems due to defects that may cause image artifacts, scanning interruptions, or sharp edges.
Product
uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This system is intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning and treatment response evaluation for diseases and…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V492000·2020-08-19
Spartan Fire Gladiator Recalled for Excessively Bright Exterior Lights
Spartan Fire is recalling one 2018 Gladiator vehicle because its exterior LED lights may be too bright, potentially blinding other drivers and increasing crash risk.
Product
SPARTAN FIRE — SPARTAN FIRE GLADIATOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2785-2020·2020-08-19
Flower Orthopedics Recalls Calcaneus Plates Due to Incorrect Material Usage
Flower Orthopedics is recalling 25 calcaneus plates because the contract manufacturer used a titanium alloy instead of pure titanium.
Product
Calcaneus Plate, Extensile, Small, Right, Catalog Number CPF 201 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2771-2020·2020-08-19
Ortho Clinical Diagnostics Recalls VITROS Anti-SARS-CoV-2 IgG Reagent Packs
Ortho Clinical Diagnostics is recalling VITROS Anti-SARS-CoV-2 IgG Reagent Packs because swapped reagent bottles may cause false negative or delayed results.
Product
VITROS Anti-SARS-CoV-2 IgG Reagent Pack, COV2IgG, VITROS CoV2G. Catalog number 6199919, UDI 10758750033355 - Product Usage: Rx ONLY. For in vitro diagnostic and Laboratory Professional use. For emergency authorization use only.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·20167·2020-08-19
Lithonia Lighting Recalls CFMK Surface Mount Brackets Due to Impact Hazard
Lithonia Lighting is recalling CFMK Surface Mount Brackets because they can fail to secure CPANL LED fixtures, causing them to fall and pose an impact injury risk.
Product
CFMK Surface Mount Brackets
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2776-2020·2020-08-19
Luminex Verigene Processor SP Recalled for Potential False Negative Results
Luminex is recalling Verigene Processor SP systems because an instrument failure may cause false negative results in blood culture tests.
Product
Verigene Processor SP with assay Luminex, VERIGENE Gram-Negative Blood Culture Nucleic Acid Test, BC-GN, IVD - Product Usage: utilizes a single-use disposable test consumables and a self-contained Verigene Test Cartridge for each sample tested.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2782-2020·2020-08-19
Flower Orthopedics Recalls Calcaneus Plates Due to Incorrect Material
Flower Orthopedics is recalling 25 calcaneus plates because they were manufactured with a titanium alloy instead of pure titanium.
Product
Calcaneus Plate, Extensile, Small, Left, Catalog Number CPF 101 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1498-2020·2020-08-19
Eosera Recalls Ear Pain MD Pain Relief Drops For Kids
Eosera, Inc. is voluntarily recalling 45,673 bottles of Ear Pain MD Pain Relief Drops For Kids due to cGMP deviations.
Product
Ear Pain MD Pain Relief Drops For Kids (lidocaine HCl Monohydrate 4%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0070-8
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2784-2020·2020-08-19
Flower Orthopedics Recalls Calcaneus Plates Due to Incorrect Material Usage
Flower Orthopedics is recalling 25 calcaneus plates because the manufacturer used a titanium alloy instead of pure titanium.
Product
Calcaneus Plate, Extensile, Large, Left, Catalog Number CPF 103 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1494-2020·2020-08-19
FDA Recalls Nystatin Oral Suspension Due to Subpotent Drug Levels
Pharmaceutical Associates, Inc. is recalling Nystatin Oral Suspension because it failed potency testing. Patients should consult their healthcare provider.
Product
NYSTATIN — NYSTATIN (NYSTATIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1154-2020·2020-08-19
Hostess Raspberry Zingers Recalled for Potential Mold Growth
Hostess Brands is recalling 34,409 cases of Raspberry Zingers cakes nationwide due to potential mold growth prior to the best-by date.
Product
Hostess Raspberry Zingers, Raspberry Iced Cake With Creamy Fillling, packaged in the following ways: 1) in boxes containing 10 cakes Net Wt. 13.4 OZ (380 g) UPC 88109110604 and 2) in clear plastic bags containing 3 cakes Net Wt. 4.02 OZ (114 g) UPC 888109010089
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2786-2020·2020-08-19
Flower Orthopedics Recalls Calcaneus Plates Due to Incorrect Material
Flower Orthopedics is recalling 25 calcaneus plates because the manufacturer used a titanium alloy instead of pure titanium.
Product
Calcaneus Plate, Extensile, Medium, Right, Catalog Number CPF 202 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2779-2020·2020-08-19
HealthFirst STAT KIT Z-1000 Emergency Medical Kits Recalled for Missing Component
HF Acquisition Co. LLC is recalling two STAT KIT Z-1000 emergency medical kits because they are missing a hand suction pump component.
Product
STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: is intended to prepare physicians with advanced cardiac life support devices and medications to respond to cardiopulmonary medical emergencies until EMS arrives.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1492-2020·2020-08-19
Teva Recalls Lidocaine Patches Due to Missing Lot and Expiration Dates
Teva Pharmaceuticals is recalling Lidocaine 5% Patches because individual pouches are missing lot and expiration dates. The recall covers 28,596 cartons distributed nationwide.
Product
LIDOCAINE — LIDOCAINE (LIDOCAINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2787-2020·2020-08-19
Flower Orthopedics Recalls Calcaneus Plates Due to Incorrect Material Usage
Flower Orthopedics is recalling 25 Calcaneus Plates, Extensile, Large, Right (Catalog Number CPF 203) because the contract manufacturer used a titanium alloy instead of pure titanium.
Product
Calcaneus Plate, Extensile, Large, Right, Catalog Number CPF 203 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1496-2020·2020-08-19
Taro Recalls Clobetasol Propionate Cream Due to Content Uniformity Failure
Taro Pharmaceuticals is recalling specific lots of Clobetasol Propionate Cream 0.05% because the bulk material failed content uniformity testing.
Product
Clobetasol Propionate Cream USP, 0.05%, a) 15 g tube, NDC: 60429-902-15; b) 45 g tube, NDC: 60429-902-45, Rx Only, For External Use Only, Not for Ophthalmic Use, Mfd by: Taro Pharmaceuticals Inc. Brampton, Ontario, Canada L6T 1C1, Marketed by: Golden State Medical Supply, Inc.…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1502-2020·2020-08-19
Lupin Recalls Mibelas 24 Fe Tablets Due to Impurity Test Failures
Lupin Pharmaceuticals is recalling Mibelas 24 Fe chewable tablets because they failed impurity specifications. The recall covers 560,922 pouches distributed nationwide.
Product
Mibelas 24 Fe (norethindrone acetate and ethinyl estradiol tablets and ferrous fumarate tablets) chewable,1 mg/0.02 mg/75 mg, Rx Only, Provides 24 days of active therapy, Pouch Contains one wallet of 28 tablets, NDC: 68180-911-11, Carton contains 3 wallets of 28 tablets each…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2798-2020·2020-08-19
FDA Recalls Barricaid Annual Closure Devices Due to Labeling Error
Intrinsic Therapeutics is recalling 110 units of Barricaid Annual Closure Devices because the inner container labels display the wrong catalog number.
Product
Barricaid Annual Closure Device (ACD) BAR-A8-8MM - Product Usage: The Barricaid¿ ACD is indicated for reducing the incidence of reherniation, and reoperation in skeletally mature patients with radiculopathy (with or without back pain) attributed to a posterior or posterolateral…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2796-2020·2020-08-19
Wright Medical Hardware Removal Kit Recalled for Missing Drivers
Wright Medical Technology is recalling 66 hardware removal kits because they lack the specific drivers needed to remove Dart-Fire 2.5 and 3.0mm Headless screws.
Product
Hardware removal kit, Part Number 1985KIT1 - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles and a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2777-2020·2020-08-19
Smith & Nephew Recalls Misidentified PeriLoc Targeter Handle
Smith & Nephew is recalling 3 units of a PeriLoc Targeter handle that was incorrectly marked as a left-hand part.
Product
PERI-LOC TARGETER 4.5MM DISTAL FEMUR, HANDLE, LEFT, NON-STERILE - Product Usage: used for adult and pediatric patients, as well as patients with osteopenic bone. PERI-LOC plates and screws are indicated for fixation of pelvic, small and long bone fractures, including those of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2783-2020·2020-08-19
Flower Orthopedics Recalls Calcaneus Plates Due to Incorrect Material
Flower Orthopedics is recalling 25 calcaneus plates because they were manufactured with a titanium alloy instead of pure titanium.
Product
Calcaneus Plate, Extensile, Medium, Left, Catalog Number CPF 102 - Product Usage: intended to be used for internal fixation of fractures and reconstruction of bones of the rearfoot, including the calcaneus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1499-2020·2020-08-19
Eosera Recalls Ear Pain MD Pain Relief Drops Due to cGMP Deviations
Eosera, Inc. is voluntarily recalling 125,874 bottles of Ear Pain MD Pain Relief Drops with 4% Lidocaine due to current Good Manufacturing Practice (cGMP) deviations.
Product
Ear Pain MD Pain Relief Drops with 4% Lidocaine (lidocaine HCl Monohydrate 4%) 0.5 FL OZ (15 mL) bottles, Eosera, Inc. 5000 South Freeway Fort Worth, TX 76115, NDC 72429-0072-2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2797-2020·2020-08-19
Wright Medical Screw Removal Case Assembly Recalled for Missing Drivers
Wright Medical Technology is recalling 9 units of the Screw Removal Case Assembly because the kits do not include drivers required to remove specific headless screws.
Product
Screw Removal Case Assembly, Part Number 1985BASE - Product Usage: The Wright Medical hardware removal kit is designed to facilitate removal of both plates and screws used in foot and ankle procedures. Along with a complete range of drivers, the kit also features driver handles…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2772-2020·2020-08-19
NeuroLogica OmniTom CT Systems Recalled for Operational Shutdown Issues
NeuroLogica is recalling 35 OmniTom CT systems due to potential operational issues that could cause inadvertent shutdowns and delays in patient treatment.
Product
OmniTom Computed tomography x-ray system, Model NL5000, all NL5000 systems with software version before 05.01.01 - Product Usage: is intended to be used for x-ray computed tomography applications for anatomy that can be imaged in the 40 cm aperture, primarily head and neck.
Category
Medical Device
Distribution
Distributed nationwide