State
73,219 recalls have nationwide distribution and so reach Ohio. 11,755 additional recalls listed Ohio specifically in their distribution scope.
Of the 11,755 recalls naming Ohio we have scored against our rubric, 2,117 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,426 (21%) are Severe.
Which agencies issued them
These figures cover only the 11,755 recalls whose distribution notice names Ohio specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ice Cream House is recalling Premium Sorbet Trifle products that may be contaminated with Listeria monocytogenes. The affected products were distributed in Ohio, New Jersey, and New York.
Ice Cream House is recalling 8' and Mini Sorbet Cake products in strawberry/mango flavors due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, New Jersey, and New York.
Mini Sorbet products distributed in Ohio, New Jersey, and New York may be contaminated with Listeria monocytogenes. Consumers should not consume these products and should return them to the retailer.
Ice Cream House recalls its 10-inch cherry sorbet cake (UPC 0-91404-15111-5) distributed in Ohio, New Jersey, and New York due to potential Listeria monocytogenes contamination.
ICE CREAM HOUSE recalled a 10'' Sorbet 4 Layer Cake for potential Listeria monocytogenes contamination. Distribution was in Ohio, New Jersey, and New York.
ICE CREAM HOUSE is recalling Mini Cone ice cream products due to potential Listeria monocytogenes contamination. Affected products were distributed in Ohio, New Jersey, and New York.
Check'ice board Sorbet Pre-Cut is being recalled due to potential Listeria monocytogenes contamination. The product was distributed in Ohio, New Jersey, and New York.
ICE CREAM HOUSE is recalling Mini Sorbet Dippers because they may be contaminated with Listeria monocytogenes. The affected products were distributed in Ohio, New Jersey, and New York.
Ice Cream House is recalling Mini Ice Cream Lollies because they may be contaminated with Listeria monocytogenes. The recalled products were distributed in Ohio, New Jersey, and New York.
Ice Cream House is recalling Mini Chocolate Sorbet Tarts (UPC 0-91404-15411-6) due to potential Listeria monocytogenes contamination. Products were distributed in Ohio, New Jersey, and New York.
Dorman Products is recalling specific front suspension ball joints because the ball stud may separate, leading to loss of steering control and increased crash risk.
B.Braun NORM-JECT Luer Lock Solo 10ml sterile syringes are being recalled because the sterile blister packaging may be damaged, potentially compromising sterility. The recall affects 604,800 units distributed nationwide.
B. Braun NORM-JECT Luer Solo 10 ml sterile syringes are recalled because blister packaging may be damaged, potentially compromising sterility. Approximately 534,000 units are affected; lot numbers 22M28C8 and 23A09C8 are included.
Mini Cigars from Ice Cream House are recalled due to potential Listeria monocytogenes contamination. The products were distributed in Ohio, New Jersey, and New York.
3M is recalling 77,280 Attest biological indicators due to caps that may melt, deform, or crack during steam sterilization cycles, potentially compromising process validation.
Ice Cream House is recalling Triangle Up Strawberry Mango Vanilla ice cream sold in Ohio, New Jersey, and New York due to potential Listeria monocytogenes contamination. No illnesses have been reported.
Dental planning software exoplan 3.1 contains a filtering error that may display all surgical guide options instead of only supported ones, potentially causing patient injury.
The Aquilex Fluid Control System (Models AQL-100PBS, AQL-100P) display may freeze at maximum volume (30,000 ml) during long procedures, causing inaccurate fluid monitoring and potential fluid overload.
IO Inspired Organics Organic Raw Walnuts recalled due to undeclared cashews. The product was distributed in six U.S. states; consumers with tree nut allergies should not consume.
Ambu Inc. is recalling the aView 2 Advance Monitor because multiple impacts can cause the device to short-circuit and potentially combust the lithium-ion battery, resulting in smoke and flames.
Stryker Corporation is recalling 96 units of the expired Cinchlock SS Knotless Anchor Inserter (Part Number CAT02462, Lot 19175AE2) distributed nationwide. Expired surgical devices may not perform reliably during use.
Inmar Supply Chain Solutions recalled various medical devices nationwide due to potential rodent exposure and temperature excursions. Affected products include bandages, tampons, condoms, blood glucose monitors, adult diapers, COVID-19 test kits, and pregnancy tests.
3M is recalling specific lots of Attest biological indicators used in steam sterilization monitoring. Certain lots have caps that may melt, deform, or crack at sterilization temperatures of 132°C and 135°C, potentially compromising sterilization process verification.
3M is recalling 172,464 units of Attest biological indicators used to validate steam sterilization because caps may melt, deform, or crack during sterilization at 132°C and 135°C.
Fresenius Kabi USA has recalled Ivenix Infusion System Large Volume Pump software versions 5.0.0 and 5.0.1 due to startup time delays that may exceed 6 minutes at flow rates between 50-200 ml/hr.