State

US Virgin Islands product recalls

72,940 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: 30
Most recent: 2026-09-09

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 30 (17%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3876–3900 of 73117

ModerateFDA (Devices)·Z-0894-2026·2025-12-17
Sacroiliac fusion screws recalled over labeling claims not consistently present
Orthofix U.S. is recalling 19,431 FIREBIRD SI Fusion System units because the labeling contains claims that are not consistently present.
Product
Brand Name: FIREBIRD" SI Fusion System Product Name: FIREBIRD" SI Fusion System Model/Catalog Number: 18-1025SP 11mm X 25mm FIREBIRD SI Screw; 18-1030SP 11mm X 30mm FIREBIRD SI Screw; 18-1035SP 11mm X 35mm FIREBIRD SI Screw; 18-1040SP 11mm X 40mm FIREBIRD SI Screw; 18-1045S
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0908-2026·2025-12-17
Ureteral stent kits, 8 French, recalled over a size labeling discrepancy
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 8 Fr x 26 cm, because the actual stent size may not match the product label.
Product
BD InLay Optima Ureteral Stent Kit Size: 8 Fr. x 26 cm, Ureteral Stent Kit REF 78826
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0895-2026·2025-12-17
Titanium spacer implants recalled over labeling claims not consistently present
Orthofix U.S. is recalling 14,201 Forza Ti Spacer System units because the labeling contains claims that are not consistently present.
Product
Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 6H; 38-2007SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 7H; 38-2008SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 8H; 38-2009SP F
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0891-2026·2025-12-17
Mini PTC spacer implants recalled over labeling claims not consistently present
Orthofix U.S. is recalling 61,977 CONSTRUX Mini PTC Spacer System units because the labeling contains claims that are not consistently present.
Product
Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number: 37-3106SP 12mm W X 12mm L, 6mm H, Parallel; 37-3107SP 12mm W X 12mm L, 7mm H, Parallel; 37-3108SP 12mm W X 12mm L, 8mm H, Parallel; 37-3109SP 12mm W X 12mm L
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0912-2026·2025-12-17
Hemodialysis systems recalled because a screw may loosen or fall out
Nipro Medical is recalling Surdial DX Hemodialysis Systems because a screw may loosen or fall out of the system.
Product
Hemodialysis System, Surdial DX REF: MC+SDX01 Rx Only
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0907-2026·2025-12-17
Ureteral stent kits recalled because the stent size may not match the label
C.R. Bard is recalling 116 BD InLay Optima Ureteral Stent Kits, 6 Fr x 30 cm, because the actual stent size may not match the product label.
Product
BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm, Ureteral Stent Kit REF 788630
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0896-2026·2025-12-17
Titanium spinal spacers recalled over labeling claims not consistently present
Orthofix U.S. is recalling 40,956 CONSTRUX Mini Ti Spacer System units because the labeling contains claims that are not consistently present.
Product
Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6006SP 12mm W X 12
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0889-2026·2025-12-17
Immunoassay reaction vessels recalled over manufacturing deformities causing instrument errors
Beckman Coulter is recalling 38,225 Access 2 Reaction Vessels because certain lots may have a small protrusion or hair-like deformity that can cause instrument errors and delay patient results.
Product
Access 2 Reaction Vessels, individual, disposable, plastic tubes used to process patient, quality control and calibration samples on the Access 2 Immunoassay system, Catalog Number 81901
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0905-2026·2025-12-17
Short ureteral stent kits recalled over a size labeling discrepancy
C.R. Bard is recalling 116 Bard InLay Optima Ureteral Stent Kits, 6 Fr x 14 cm, because the actual stent size may not match the product label.
Product
Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0909-2026·2025-12-17
AMSCO 7052HP washer disinfectors recalled over a wire that may shift
Steris is recalling 10 AMSCO 7052HP Washer/Disinfectors because a wire connected to the electrical box may shift out of position, which may result in electrical arcing inside the unit.
Product
AMSCO 7052HP Washer/Disinfector Model/Catalog Number: 7052HP Product Description: The AMSCO 7052HP Washer/Disinfector is intended for use in the cleaning and intermediate-level disinfection of soiled reusable simple hard-surfaced rigid surgical instruments (such as forceps a
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0918-2026·2025-12-17
Bariatric hospital beds recalled because they are not tested with certain mattresses
Stryker is recalling 294 MV3 bariatric beds because they and Arise 1000EX mattresses have been sold in close proximity, and the two products have not been tested for compatibility.
Product
Stryker MV3 bariatric bed, Part Number 5900000001
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0227-2026·2025-12-17
Sertraline tablets recalled because bottle seals are not adhering
Lupin Pharmaceuticals is recalling 52,128 bottles of Sertraline Hydrochloride Tablets, 100 mg, over a defective container in which the seal is not adhering to the bottles.
Product
SERTRALINE HYDROCHLORIDE — SERTRALINE HYDROCHLORIDE (SERTRALINE HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0906-2026·2025-12-17
Ureteral stent kits, 4.7 French, recalled over a size labeling discrepancy
C.R. Bard is recalling 4,350 BD InLay Optima Ureteral Stent Kits, 4.7 Fr x 26 cm, because the actual stent size may not match the product label.
Product
BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm, Ureteral Stent Kit REF 788426
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0217-2026·2025-12-17
Lanthanum carbonate tablets recalled in a second hardness specification failure
Cipla USA is recalling 1,180 boxes of Lanthanum Carbonate chewable tablets, 1000mg, from a further lot after an out of specification hardness test result.
Product
LANTHANUM CARBONATE — LANTHANUM CARBONATE (LANTHANUM CARBONATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0219-2026·2025-12-17
Varenicline tablets recalled after an assay value fell below specification
Dr. Reddy's Laboratories is recalling 4,800 bottles of Varenicline Tablets, 1mg, after the assay value for the affected lot fell below the specification limit at nine-month stability testing.
Product
VARENICLINE TARTRATE — VARENICLINE TARTRATE (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0221-2026·2025-12-17
Compounded ophthalmic syringes recalled over an incorrect product formulation
Fagron Compounding Services is recalling 2,980 syringes of a compounded topical ophthalmic solution over an incorrect product formulation.
Product
Tropicamide 1%/Cyclopentolate 1%/Phenylephrine 2.5%/Ketorolac 0.5% Topical Ophthalmic Solution, 0.5mL Single-Use Syringe, For Topical Ophthalmic Use Only. Not for IV Use. Fagron Sterile Services, 8710 E 34th St N, Wichita, KS 67226. NDC: 71266-8240-01
Category
Drug
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0917-2026·2025-12-17
Balloon pump systems recalled with a revised preventative maintenance schedule
Datascope is recalling 47 Cardiosave Rescue Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Product
Cardiosave Rescue. Intra-Aortic Balloon Pump system.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0916-2026·2025-12-17
Hybrid balloon pumps recalled with a revised preventative maintenance schedule
Datascope is recalling 11,470 Cardiosave Hybrid Intra-Aortic Balloon Pump systems to issue an instructions for use addendum revising the preventative maintenance schedule.
Product
Cardiosave Hybrid. Intra-Aortic Balloon Pump system.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V869000·2025-12-16
Toyota hybrid inverter bolt can loosen causing power loss or fire
Toyota is recalling certain 2025-2026 Camry Hybrid and 2026 Corolla Cross Hybrid vehicles because a bolt inside the inverter may not be tightened properly, causing incomplete contact at the terminal.
Product
TOYOTA — TOYOTA CAMRY HYBRID, COROLLA CROSS HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V870000·2025-12-16
Gillig Recalls 2025 Low Floor Buses Due to Wheelchair Restraint Defect
Gillig is recalling 2025 Low Floor transit buses because wheelchair restraints may fail to lock, posing an injury risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V867000·2025-12-15
Mack Trucks Recalls 2010-2016 Granite Trucks Due to Brake Imbalance Risk
Mack Trucks is recalling 2010-2016 Granite trucks because incorrect parts from a previous repair may cause brake overheating, increasing the risk of tire blowouts or fires.
Product
MACK — MACK GRANITE (GU)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V868000·2025-12-15
Gillig Recalls 2013 Low Floor Transit Buses for Emergency Exit Defect
Gillig is recalling 2013 Low Floor transit buses because emergency exit window latches may fail during a crash, increasing injury risk.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·038-2025·2025-12-12
Suzanna's Kitchen Recalls Breaded Chicken for Undeclared Soy Allergen
Suzanna's Kitchen is recalling fully cooked breaded chicken products because they contain soy, a known allergen, that is not declared on the label.
Product
Suzanna's Kitchen — Suzanna’s Kitchen Recalls Fully Cooked Breaded Chicken Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·25V860000·2025-12-12
Ford Recalls 2022-2025 E-Transit Vehicles Due to Axle Shaft Defect
Ford is recalling 2022-2025 E-Transit vehicles because the left rear axle half shaft may disengage, causing loss of drive power or vehicle rollaway.
Product
FORD — FORD E-TRANSIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V866000·2025-12-12
Ford Super Duty trucks recalled over rear axle shafts that may break
Ford is recalling 6,819 model year 2026 Super Duty F-250 and F-350 vehicles because the right rear axle shaft may have been improperly heat-treated and may break.
Product
FORD — FORD F-250 SD, F-350 SD
Category
Vehicle
Distribution
Distributed nationwide