State
72,986 recalls have nationwide distribution and so reach Virginia. 9,483 additional recalls listed Virginia specifically in their distribution scope.
Of the 9,483 recalls naming Virginia we have scored against our rubric, 1,286 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,296 (24%) are Severe.
Which agencies issued them
These figures cover only the 9,483 recalls whose distribution notice names Virginia specifically. The 72,986 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Volvo Bus is recalling 2023-2025 9700 buses because metallic debris in fire suppression connectors may cause engine shutdowns and false alarms.
Edwards FEM-FLEX II Femoral Arterial Cannulas are being recalled after complaints of a 3 mm to 4 mm section of wire exposed or protruding from the outside of the cannula body. 847 units affected.
Weaver Chocolates Nonpareil Semi-Sweet Chocolate in 25 lb bulk cases is being recalled because of an undeclared milk allergen. 849 cases are affected.
Wegmans brand Chocolate Chip Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.
Wegmans brand Blueberry Mini Muffins family pack is being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.
Torflex Transseptal Guiding Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.
Alcon Constellation Vision System Combined Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 89,495 units affected.
Alcon Custom Paks, customer-designed sterile surgical kits, are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 15,557 kits affected.
Wegmans Semi-Sweet Chocolate Nonpareils are being recalled because of undeclared milk. 595 cases are affected across nine states and the District of Columbia.
VersaCross Transseptal Sheath Kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.
Alcon Constellation Vision System Vitrectomy Procedure Paks are being recalled because some units within specific lots may have been damaged during manufacture in the lidding area. 198,205 units affected.
Infinia, Infinia Hawkeye, Infinia II and Infinia II Hawkeye 4 nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software. 1,822 units affected.
VersaCross Access Solution kits are being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units affected.
The O-arm O2 Imaging System is being recalled because a mechanical component supporting the gantry to the support structure may have been damaged during manufacture. 3 units affected.
The VersaCross RF Wire is being recalled because of a potential hole in the Tyvek layer of the sterile barrier pouch, which may compromise device sterility. 14,724 units are affected.
Varicam, Millennium VG, Millennium VG Hawkeye and Discovery VH nuclear medicine systems are being recalled because unintended radial detector motion may occur without the correct gantry software version. 21 units affected.
Wegmans brand French Toast Mini Muffins are being recalled because the product may contain foreign objects of metal origin. 8,508 units are affected.
Duloxetine Delayed-Release Capsules 40 mg are being recalled because N-nitroso-duloxetine was present above the FDA recommended interim limit. 12,242 bottles are affected.
TrueDent Magenta dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 94 units are affected.
TrueDent White dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 109 units are affected.
Preat Astra EV-compatible 4.2 mm Digital Analogs are being recalled because a manufacturing error left the digital analog rotational feature 180 degrees off. 44 units are affected.
TrueDent Clear dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 78 units are affected.
TrueDent Cyan dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 100 units are affected.
Famciclovir Tablets USP 500 mg from Macleods Pharma are being recalled because a black hair strand was found attached to a tablet in a sealed bottle. 9,888 bottles are affected.
TrueDent Yellow dental resin cartridges are being recalled because a formatting error switches the day and month in the expiration date. 68 units are affected.