State
72,940 recalls have nationwide distribution and so reach Wisconsin. 8,408 additional recalls listed Wisconsin specifically in their distribution scope.
Of the 8,408 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 1,957 (23%) are Severe.
Which agencies issued them
These figures cover only the 8,408 recalls whose distribution notice names Wisconsin specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Medline is recalling the 120-inch latex-free ExtendFlex anesthesia circuit after complaints of leaks caused by cracks in the expandable tubing. The FDA has classified it Class I.
Cerenovus is recalling 12,004 CEREPAK Detachable Coil System units because the coils may fail to detach, which could result in hemorrhagic and ischemic stroke. The FDA classified it Class I.
Medline is recalling the latex-free Breathing Kit DYNJ10550 after complaints of anesthesia circuit leaks caused by cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom Red Bali powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom Bali Gold powder in 4 oz and 8 oz sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom White Elephant powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Medline is recalling open heart supplement and vascular kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Lotus Vaping Technologies is recalling Monarch Premium Kratom Green Maeng Da powder in three sizes because the product may be contaminated with Salmonella. The FDA classified it Class I.
Medline is recalling ENT and laryngoscopy-bronchoscopy kits containing anesthesia circuits after complaints of leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Medline is recalling multiple adult 120-inch expandable anesthesia circuits after complaints of leaks caused by cracks in the tubing. The FDA has classified it Class I.
Medline is recalling robotic gastric sleeve, cysto and general laparoscopy kits after complaints of anesthesia circuit leaks from cracks in the 120-inch expandable tubing. The FDA classified it Class I.
Tiffin Motorhomes, Inc. is recalling certain 2026 Open Trail motorhomes because the cargo carrying capacity labels may be incorrect, which could lead to vehicle overloading.
Medline is recalling 18,117 reprocessed LigaSure Small Jaw instruments because certain areas of the device can trap residual material that may become dislodged.
Techno-Path is recalling 51 units of Multichem ID-B positive control serum from a second lot because of potential negative recovery of the HBsAg analyte on the Alinity i platform.
Olympus is recalling 18,174 Single Use Electrosurgical Snares SD-400U-15 because sterility may be compromised by small holes formed during packaging or transportation.
Shimadzu is recalling 1,766 ceiling type X-ray tube supports, models CH-200 and CH-200M, because the mounting shaft may break and the tube assembly could come off.
GE Healthcare is recalling 7,408 B105P, B125P, B105M, B125M and B155M patient monitors because certain batteries can lose the ability to hold charge, causing a loss of monitoring.
Professional Botanicals is recalling 430 bottles of Total Comfort capsules because the product contains magnesium salicylate.
GE Healthcare is recalling 5,935 CARESCAPE ONE patient monitors because certain batteries can lose the ability to hold charge, causing a loss of patient monitoring.
Medline is recalling 4,226 reprocessed LigaSure Exact dissectors, 21 cm, because certain areas of the device can trap residual material that may become dislodged.
Orthofix is recalling 624 Virata preassembled polyaxial screws used in the Virata Spinal Fixation System because the screws do not meet performance standards.
Medline is recalling one reprocessed LigaSure Impact Curved Large Jaw sealer/divider because certain areas of the device can trap residual material that may become dislodged.
Abbott Laboratories is recalling 833 Alinity hq Analyzers because a software issue means the system does not visibly flag results when saturation is present, which may give incorrect results.
Medline is recalling 4,007 reprocessed LigaSure Maryland Jaw sealer/dividers, 23 cm, because certain areas of the device can trap residual material that may become dislodged.
Medline is recalling 57,244 reprocessed LigaSure Maryland Jaw sealer/dividers because certain areas of the device can trap residual material that may, in rare cases, become dislodged.