State
73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The FDA is recalling 7-Ment Alpha Advanced Mass Builder capsules because they contain an unapproved synthetic hormone ingredient.
Detox Transforms is recalling BtRiM Max capsules because they contain undeclared phenolphthalein, making the product an unapproved drug.
Anabolic Science Labs is recalling Professional Formexx Black capsules because they contain an unapproved synthetic hormone ingredient.
Bard Peripheral Vascular Inc is recalling 7,995 Bard MAX-CORE Disposable Core Biopsy Instruments due to a risk of self-activation-related issues.
Spiceco is recalling Emeril's Blackened Seasoning Blend because it may contain undeclared peanut protein. The recall includes 2,483 cases distributed nationwide and abroad.
Spacelabs is recalling Ultraview SL Command Modules with specific Masimo SpO2 components due to a defect causing random resets.
Stryker Instruments is voluntarily recalling Ambulating Bulbs used with wound drains because of a potential sterility breach in the packaging.
ICU Medical is recalling 5,100 units of MicroClave T-Connectors because potential connection separation issues could lead to leakage.
Spiceco is recalling Pride of Szeged Fish Rub Seasoning because it may contain undeclared peanut protein. The recall includes additional products using the implicated paprika.
Spiceco, Inc. is recalling Sylvia's Rib Rub N More Seasoning because it may contain undeclared peanut protein. The recall includes 324 cases distributed nationwide and abroad.
Spiceco is recalling Hytop Seasoned Salt because it may contain undeclared peanut protein. The recall includes specific lot numbers distributed nationwide and abroad.
Stryker Instruments is voluntarily recalling specific trocar wound drains and ambulating bulbs because of a potential sterility breach in the packaging.
Spiceco is recalling Emeril's Cajun Seasoning Blend because it may contain undeclared peanut protein. The recall includes 2,458 cases distributed nationwide and abroad.
ICU Medical is recalling 50 units of 98-inch Transfer Sets because potential connection separation could lead to leakage.
Stryker Instruments is voluntarily recalling CBCII Wound Drains and Ambulating Bulbs due to a potential sterility breach in the packaging.
Stryker Instruments is voluntarily recalling specific wound drain and ambulating bulb products due to a potential sterility breach in the packaging.
ICU Medical is recalling MicroClave T-Connectors because potential connection separation issues could lead to leakage.
Spiceco is recalling Shoppers Value Chicken Seasoning and Pride of Szeged Sweet Hungarian Paprika because they may contain undeclared peanut protein.
Spiceco is recalling Twin Tree Gardens Seasoning Salt and Pride of Szeged Paprika because they may contain undeclared peanut protein.
B. Braun Medical is recalling specific pain control trays because a potential hole in the outer tray may compromise the sterile barrier, posing a risk of contamination.
Spiceco is recalling Eagle Brand Seasoning Salt and Pride of Szeged Sweet Hungarian Paprika because they may contain undeclared peanut protein.
Spiceco is recalling Redner's Chicken Rub and Sweet Hungarian Paprika because they may contain undeclared peanut protein.
Spiceco is recalling specific lots of chicken seasoning and sweet Hungarian paprika because they may contain undeclared peanut protein.
Stryker Instruments is voluntarily recalling CBCII Wound Drains and Ambulating Bulbs due to a potential sterility breach in the packaging.
Philips is recalling EPIQ 7 Ultrasound Systems with the Pediatric Cardiology option because a unit conversion error may cause incorrect Body Surface Area calculations.