State
72,971 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.
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 72,971 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Eugia US LLC is recalling Tirofiban Hydrochloride Injection due to out-of-specification test results for related substances found during a three-month stability study under long-term storage conditions.
Accord Healthcare is recalling 4,872 bottles of Levothyroxine Sodium Tablets (50 mcg) nationwide because the tablets are subpotent and may not provide the intended therapeutic effect.
Medline procedure kits containing Sterile Water and Sterile 0.9% Normal Saline bottles are being recalled because the bottles leak at the peel-foil and bottle opening interface.
Medline is recalling Plastics Suture Tray kits (Ref SUT13535) because the included Sterile Water and Sterile 0.9% Normal Saline bottles leak at the peel-foil and bottle opening interface.
Medline Sterile Water, USP 100mL bottles are being recalled because they leak at the interface between the peel-foil and bottle opening, posing a contamination risk.
Medline Sterile 0.9% Normal Saline 100mL bottles are being recalled because they may leak at the interface where the peel-foil meets the bottle opening. The bottles were distributed nationwide in the US and in Panama and Canada.
Eugia US LLC is recalling Tirofiban Hydrochloride Injection due to out-of-specification test results for related substances found during stability testing. The affected lot was distributed nationwide.
Accord Healthcare is recalling approximately 18,984 bottles of Levothyroxine Sodium Tablets, 112 mcg, nationwide because the tablets are subpotent. Patients taking this medication should contact their pharmacy or healthcare provider immediately.
Medline procedure kits containing sterile water and 0.9% normal saline bottles are being recalled because the bottles leak at the peel-foil and bottle opening interface. The kits were distributed worldwide including the US, Panama, and Canada.
IBA Dosimetry GmbH is recalling the myQA iON dosimetry device (Article Number MQ10-000) because creating two structures with identical names except for a special character causes wrong analysis results.
Boston Scientific is recalling 435 IceSeed 1.5 CX S cryoablation needles manufactured between April 2024 and February 2025 that were programmed with DEMO settings instead of Commercial settings, which can cause the Cryoablation System to prompt repeated tests if the needle is disconnected and reconnected.
Preferred Pharmaceuticals, Inc. is voluntarily recalling Clindamycin Hydrochloride Capsules USP 300mg due to manufacturing process deviations. The recall affects 1190 bottles distributed nationwide.
Boston Scientific is recalling IceSeed 1.5 CX cryoablation needles manufactured between April 2024 and February 2025 due to incorrect software programming. Affected needles may prompt unnecessary Needle Integrity and Functionality Tests if disconnected and reconnected during use.
Medline Industries is recalling Sterile Water and Sterile 0.9% Normal Saline bottles due to leaking at the peel-foil and bottle opening interface. The affected kits were distributed nationwide and internationally.
Accord Healthcare is recalling 4,888 bottles of Levothyroxine Sodium Tablets (25 mcg) nationwide due to subpotency. The affected lot is D2300323 with expiration date 01/2026.
Boston Scientific is recalling IceSeed 1.5 CX S cryoablation needles manufactured April 2024 to February 2025 that were programmed with DEMO instead of Commercial settings. If disconnected and reconnected after initial testing, the system will re-prompt testing rather than functioning normally.
Hyundai is recalling certain 2025 Palisade vehicles because an insufficient seal on the electric oil pump controller can allow moisture to accumulate and cause an electrical short that may result in fire. Owners should park vehicles outside and away from structures until the repair is completed.
KZRV is recalling 2025 Durango Gold fifth wheels because removable step brackets may loosen, causing steps to detach and increasing injury risk.
Grand Design is recalling certain 2024–2025 Momentum toy haulers with removable step assemblies because the clip-on bracket mounting bolts may loosen, causing the steps to detach and increase the risk of injury.
Blue Bird is recalling 2026 Vision and All American school buses because seat mounting fasteners may be improperly tightened, increasing injury risk in crashes.
Prevost is recalling one 2025 X3-45 VIP Entertainer because front lower control arm fasteners may be improperly tightened, risking vehicle control loss.
Porsche is recalling certain 2022 and 2023 Taycan vehicles because an occupant classification system error may deactivate the front passenger air bag, increasing injury risk in a crash.
Tiffin is recalling 2025 Zephyr motorhomes because the secondary emergency exit is on the same side as the primary exit, increasing injury risk.
Altec Industries is recalling certain 2022-2024 Aerial Devices because fuel lines may not be properly secured, potentially causing fuel leaks and fire risk when an ignition source is present.
Mercedes-Benz is recalling certain 2022-2025 C 300 and 2023-2024 AMG C 43 vehicles. The driver-side seat belt cover may not be properly installed, potentially causing the seat belt anchor to loosen.