State
73,566 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.
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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Bamamon is recalling LED Projecting Finger Light Toys because the button cell batteries pose a risk of serious injury or death if ingested.
Costway is recalling convertible high chairs that lack a passive restraint system, creating a risk of serious injury or death from entrapment or falls.
The CPSC is recalling CIYTI Light-Up Princess Costumes because accessible button batteries pose a risk of serious injury or death if swallowed. Consumers should stop using the costumes and contact the seller for a refund.
VQQQ natural gas patio heaters are being recalled because malfunctioning components can release gas, posing a risk of serious injury or death from fire and burns.
Lithonia Lighting is recalling RSX luminaires with specific adjustable tilt arm mountings because the knuckle can fail, causing the fixture to fall and pose a risk of serious injury.
Koenigsegg is recalling 2025-2026 CC850 vehicles because the electronic parking brake may not engage in reverse, increasing crash risk.
Instrumentation Laboratory is recalling 434 units of the HemoslL AcuStar HIT-lgG in vitro diagnostic due to potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.
SI-BONE, Inc. is recalling 100 units of iFuse TORQ Implant System screws because packaging seal integrity testing failed, preventing assurance of sterility.
Jenavalve Technology Inc. is recalling 143 JenaValve Trilogy Delivery Catheters due to a defect that may prevent heart valve deployment.
Beckman Coulter is recalling DxU 840m and 850m Iris analyzers because a check valve defect can cause fluid leaks, creating slip, chemical, and biohazard risks.
Medtronic is recalling 18 units of Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.
Ethicon is recalling 1,764 units of PERMA-HAND Silk sutures that were packaged with alcohol-based fluid. The fluid is not part of the product design and could cause surgical delays or treatment failure if used.
Zydus Pharmaceuticals is recalling 70,776 vials of Hydrocortisone Sodium Succinate for Injection due to failed impurities and degradation specifications.
Steris Corporation is recalling 374 units of RAPICIDE PA Part A High-Level Disinfectant because a blocked vented cap may cause the bottle to swell and release vapor or liquid, posing an injury risk.
Houston Rx LLC is recalling 64 vials of Tirzepatide/Niacinamide injection due to a lack of assurance of sterility. The product was distributed nationwide.
Medline is recalling 56 surgical convenience kits because the cannula components may leak or break during use.
Steris is recalling 11,806 units of its RAPICIDE PA high-level disinfectant because a blocked vented cap can cause the bottle to swell and release vapor or liquid, risking user injury.
Medline Industries is recalling 36,199 surgical convenience kits nationwide because cannula components do not meet ISO 80369-7 dimensional requirements, posing a risk of leaking or breaking during use.
Becton Dickinson is recalling 669,200 units of the BD Phoenix Panel NMIC-306 due to potential quality control failures with Klebsiella pneumoniae ATCC BAA-1705.
Cadwell Industries is recalling 23 IOMAX Cortical Modules because a defective circuit board may cause unintended electrical stimulation to patients.
Audi is recalling 2024-2025 Q4 E-Tron and Q4 Sportback E-Tron vehicles because the high-voltage battery may fail and cause a fire.
Jenavalve Technology Inc. is recalling 111 units of JenaValve Trilogy Delivery Catheters due to a defect that may prevent heart valve deployment.
Instrumentation Laboratory is recalling 1,414 units of HemoslL AcuStar HIT-lgG(PF-4) in vitro diagnostic reagents due to a potential for invalid calibration curves or negative mean bias of up to 47% with patient samples.
Jenavalve Technology Inc. is recalling 108 units of the JenaValve Trilogy Delivery Catheter due to a defect that may prevent heart valve deployment.
Medtronic is recalling specific Grafton DBM and Grafton Plus DBM products because the donor tissue tested positive for Clostridium butyricum, posing a potential infection risk.