State
72,820 recalls have nationwide distribution and so reach Wisconsin. 8,407 additional recalls listed Wisconsin specifically in their distribution scope.
Of the 8,407 recalls naming Wisconsin we have scored against our rubric, 1,547 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,956 (23%) are Severe.
Which agencies issued them
These figures cover only the 8,407 recalls whose distribution notice names Wisconsin specifically. The 72,820 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Apollo Care, LLC is recalling specific lots of Semaglutide 6.75mg vials because they contain nylon and silk-type particulate matter.
Apollo Care is recalling 250 vials of Semaglutide 7.5mg due to the presence of nylon and silk-type particulate matter.
Apollo Care, LLC is recalling 250 vials of Semaglutide 5mg due to the presence of nylon and silk-type particulate matter.
Taylor Farms de Mexico is recalling specific lots of shredded iceberg lettuce due to potential Cyclospora contamination. The product was distributed across 28 U.S. states and Mexico.
FDA is recalling Surgipro II sutures due to potential sterile packaging defects that could cause biocontamination and infection.
Shoolin Pharma Chem LLP is recalling Tadalafil USP 1.00 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Erbe USA Inc is recalling ERBECRYO 2 Cryosurgical Units because a strong pull on the high-pressure transfer hose may cause the cryoprobe to rupture.
Apollo Care, LLC is recalling 4,748 vials of Semaglutide 0.9mg due to the presence of nylon and silk particulate matter.
529 Commerce, LLC is recalling Aquafaba Powder, Vegan Replacement, because it contains undeclared egg. The product was distributed to 24 states.
Taylor Farms is recalling specific lots of Subway Shred Lettuce due to potential Cyclospora contamination. The product was distributed to 28 US states and Mexico.
Baxter Healthcare is recalling 19,032 bags of Cefazolin Injection due to the presence of particulate matter. The affected product is distributed nationwide in the US.
Apollo Care, LLC is recalling 500 vials of Semaglutide 10mg due to the presence of nylon and silk-type particulate matter.
Taylor Farms is recalling specific Cross Valley Farms lettuce products due to potential Cyclospora contamination. Consumers should check lot codes and discard or return affected items.
Taylor Farms is recalling specific Marketside iceberg salad products due to potential Cyclospora contamination. Consumers should check lot codes and discard affected items.
Taylor Farms de Mexico is recalling specific lots of iceberg and romaine lettuce blends due to potential Cyclospora contamination.
Taylor Farms is recalling specific lots of garden salad mix and lettuce blends due to potential Cyclospora contamination. Consumers should check lot codes and discard affected products.
FDA is recalling Surgipro sutures due to potential sterile barrier defects that could cause biocontamination and infection.
Shoolin Pharma Chem LLP is recalling Tadalafil USP 0.500 KG bags due to Current Good Manufacturing Practice (CGMP) deviations noted during an FDA inspection.
Cardinal Health is recalling 602 Presource surgical kits because they contain MEDICOM Ritmed Neurological Sponges with unexpected endotoxin variability.
Baxter Healthcare is recalling 24,528 units of Duo-Vent Solution Sets due to customer reports of air bubbles in the drip chamber and tubing.
FDA is recalling V-Loc 180 Absorbable Wound Closure Devices due to potential sterile barrier packaging defects that could lead to biocontamination.
Cardinal Health is recalling Presource Kits containing MEDICOM Ritmed Neurological Sponges due to unexpected variability in endotoxin levels.
Apollo Care, LLC is recalling specific lots of Semaglutide 9mg vials because they contain nylon and silk-type particulate matter.
Philips is recalling 4,252 Allura Xper FD interventional fluoroscopic x-ray systems worldwide due to a firmware issue that may cause loss of geometry movements.
BioFire Diagnostics is recalling 2,370 pouches of the BIOFIRE Respiratory Panel 2.1 test due to an increase in false negative results.