State
73,213 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 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
TJX is recalling about 10,850 Haining Degao Benches because the legs can break or detach when someone is seated, creating a fall hazard. The company has received 21 reports of legs breaking or detaching at stores, including 17 reports of injuries.
Uniek is recalling Kate and Laurel Astora and Valenti mirrors because the mirror glass can detach from the frame and fall, posing a laceration hazard. No injuries have been reported.
Little Cotton Clothes children's pajamas and nightdresses fail to meet federal flammability standards for sleepwear, posing a burn injury risk. About 550 units were sold online and in children's clothing stores from September 2022 through January 2023.
TopGlore is recalling about 650 Narskido infant bath seats sold on Amazon because they fail to meet federal safety standards and can tip over, posing a drowning hazard to babies.
Chrysler is recalling 2022 Jeep Grand Cherokee 4XE vehicles because a software issue may cause the engine to shut down, increasing crash risk.
BMW is recalling 2023 740i, 760i, and i7 vehicles because front seat length adjustment systems may not be welded properly, increasing injury risk in a crash.
John Deere is recalling about 1,600 XUV590E, XUV590M, and XUV590M S4 Gator utility vehicles because fuel can leak from under the fuel cap, creating a fire hazard. No injuries have been reported.
Nissan is recalling driver-side powered seat cushion frames for certain 2021-2023 Rogue, Pathfinder, and INFINITI QX60 vehicles because the seat may not be fully secured, increasing injury risk in a crash.
Akorn, Inc. is recalling all lots of Diuril (chlorothiazide sodium) Injection, 500mg/vial, distributed nationwide, due to manufacturing deviations. The manufacturer went out of business and was unable to complete required stability studies.
Akorn, Inc. is recalling all lots of Lactulose Solution USP (Oral), 10g/15mL, distributed nationwide in the USA and Puerto Rico, due to the manufacturer's inability to complete required stability studies following company closure.
Akorn, Inc. is recalling all lots of Hydromorphone Hydrochloride Injection due to CGMP deviations. The firm went out of business and could not complete required stability testing.
Akorn, Inc. is recalling all lots of Valproic Acid Oral Solution, USP (250mg/5mL) nationwide. The recall was issued because the firm ceased operations and could not complete required stability studies as mandated by manufacturing regulations.
Akorn, Inc. is recalling all lots of Lidocaine HCl Jelly USP 2% in 5mL tubes nationwide due to manufacturing quality control violations. The company ceased operations and could not complete required stability testing.
Akorn is recalling all lots of Artificial Tears Ointment nationwide due to manufacturing compliance deviations. The company went out of business and was unable to complete required stability studies.
Akorn recalled all lots of Megestrol Acetate Oral Suspension nationwide due to the firm's inability to complete required stability studies after ceasing operations.
Akorn Inc. is recalling all lots of Sufenta (Sufentanil Citrate Injection) distributed nationwide. The manufacturer ceased operations and could not complete required stability studies to verify drug safety and effectiveness over time.
Akorn recalls all lots of Tropicamide Ophthalmic Solution 0.5% (15 mL bottles) nationwide due to CGMP deviations. The firm was unable to complete required stability studies after ceasing operations.
Maquet is recalling QUADROX-i Adult cardiopulmonary bypass oxygenators (Models HMO 70000-USA and HMO 71000-USA) due to packaging defects including holes, cracks, and improper placement of accessories that may compromise sterility.
Denison Pharmaceuticals recalls Pin-Away Pyrantel Pamoate pinworm treatment nationwide due to CGMP deviation: non-food-grade lubricant used in the manufacturing mixing vessel.
Kia is recalling certain 2023 Sportage vehicles where the brake booster diaphragm may become misaligned, causing a loss of power brake assist and extending vehicle stopping distance.
Akorn, Inc. is recalling all lots of Midazolam Injection USP 2mg/2mL nationwide because the manufacturer went out of business and cannot complete required stability studies mandated by Current Good Manufacturing Practice regulations.
Maquet Medical Systems USA is recalling 1,784 QUADROX-i Small Oxygenators due to packaging defects that may compromise the sterile barrier, risking infection and other serious complications.
Maquet is recalling QUADROX-i Adult Oxygenators used in cardiopulmonary bypass surgery due to packaging defects that may compromise the sterile barrier. Contact with non-sterile devices could cause infection, sepsis, or ischemia.
BMW is recalling 2022-2024 iX vehicles because cruise control may unintentionally reactivate when turning the steering wheel at low speeds, increasing the risk of unintended acceleration and crashes.
Akorn, Inc. is recalling all lots of Tobramycin Ophthalmic Solution 0.3% because the manufacturer went out of business and could not complete required stability studies, a violation of manufacturing regulations.