State
20,371 recalls have nationwide distribution and so reach Wisconsin. 0 additional recalls listed Wisconsin specifically in their distribution scope.
Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Wisconsin consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.
If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.
Myx is recalling approximately 162,000 MYX I, MYX II, and MYX II Plus exercise bicycles because pedals can loosen or detach during use, causing injury. Myx has received 864 reports of pedal loosening or detachment, including 75 injury reports involving bruises and cuts.
Keystone is recalling 2021-2022 Sprinter and Bullet models plus multiple 2022 travel trailer and fifth-wheel variants due to faulty solar controller wiring that can disable carbon monoxide and propane gas detectors.
Rad Power Bikes is recalling about 29,300 RadWagon 4 electric cargo bikes because the tires can unexpectedly go flat or separate, risking falls and crashes. The firm has received 137 reports of tire failures and eight injury reports.
Tangame Busy Houses, wooden activity toy cubes sold on Amazon, contain lead paint on a zipper, lead in a plastic phone cord, and phthalates in a horn bulb, exceeding federal safety bans. No injuries have been reported.
Ford is recalling 2021-2022 Edge vehicles with a software error that may cause the rearview camera to display a blank or distorted image. This reduces driver visibility behind the vehicle, increasing crash risk.
BS Interactive is recalling Stashables Finger Skateboard Ramp Sets because the miniature skateboards and scooters contain lead paint levels exceeding federal limits and fail lead content bans, posing a lead poisoning risk to young children.
FHS Retail is recalling about 1,700 units of FUUL 1.9L Pure Liquid Paraffin Lamp Oil because the packaging is not child-resistant and the label omits mandatory safety information required by federal law. The product can cause fatal chemical pneumonia or lung damage if ingested.
Clarks Americas is recalling three styles of women's navy canvas shoes sold from February to October 2022 because prolonged contact with the shoe material can expose wearers to toxic chemicals benzidine and/or dimethoxybenzidine.
Nationwide recall of 8.4% sodium bicarbonate injection vials due to container defects causing vial breakage and glass fragments when pressurized during preparation.
Golden State Medical Supply Inc. is recalling 2,584 bottles of Atenolol 25mg tablets nationwide. Bottles labeled as Atenolol 25mg actually contain Clopidogrel 75mg tablets—a different medication.
Exela Pharma Sciences is recalling 2,123,040 vials of Sodium Bicarbonate 8.4% Injection due to container defects causing vial breakage and glass release when pressurized during product preparation.
Secrets of the Tribe is recalling Amla Alcohol-Free Extract (2 oz and 4 oz bottles) distributed nationwide due to elevated lead levels.
Encore Medical is recalling EMPOWR hip liner implants because boxes may contain knee inserts instead. This packaging error could delay surgeries. Four units affected in six US states.
ConvaTec is recalling 5,284 units of Esteem+ Durahesive Plus ostomy pouches due to impaired release liner functionality. The defect may affect proper device operation for patients managing colostomy or ileostomy output.
W L Gore & Associates is recalling 98 GORE CARDIOFORM ASD Occluder cardiovascular implants due to failed manufacturing release test results. Affected units were distributed nationwide and internationally.
Secrets of the Tribe is recalling Indian Gooseberry Alcohol-Free Extract (2 oz and 4 oz bottles) distributed nationwide due to elevated lead levels. Consumers should stop using the product.
Siemens is recalling ARTIS pheno x-ray systems with VE10B software due to three potential software issues that may prevent continued treatment on the affected system, potentially requiring use of an alternate system.
Ultra Chem Labs Corp is recalling Proton Armor Anti-Microbial Alcohol-Free Foaming Hand Sanitizer nationwide due to trace amounts of methanol found in product components during manufacturing. The recall affects multiple bottle sizes with batch number 20117206.
Stryker INBONE Tibial Trays are being recalled due to an oversized lock detail that could affect proper component assembly and implant function. Affected units were distributed in New York.
AuroMedics Pharma LLC is recalling 11,520 units of Fondaparinux Sodium Injection nationwide due to out-of-specification potency. Patients should contact their healthcare provider immediately.
Medline is recalling 460 Pre-Op CHG Bathing Kits because the CHG solution and blood culture bottles have expiration dates that don't match the kit label. Expired components could compromise effectiveness.
Wright Medical Technology is recalling one Stryker INBONE Tibial Tray due to an oversized tibial tray lock detail that exceeds product specifications and could affect device functionality.
ConvaTec recalled 182 units of Esteem+ Durahesive Plus ostomy pouches nationwide due to impaired release liner functionality. The defect affects pouches with batch number 2A02671 and UDI 768455115334.
ConvaTec is recalling 2,611 units of its Active Life ostomy pouch due to impaired release liner functionality. The defect may affect product performance and seal integrity.
Medline Industries is recalling 1,600 blood culture kits (Reorder # DYNDH1592) because component expiration dates don't match the kit label. Affected components include CHG Solution and Bactec bottle plastic.