State
73,824 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.
Of the 5,822 recalls naming Kansas we have scored against our rubric, 1,053 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,486 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,822 recalls whose distribution notice names Kansas specifically. The 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
All American Seasonings, Inc. is recalling 478 bags of French Onion Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.
Stryker Howmedica Osteonics Corp. is recalling 131 units of the Reunion TSA Peg Alignment Sound because the instrument broke during surgery.
All American Seasonings, Inc. is recalling 59 bags of Triple Cheese Blend due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
All American Seasonings, Inc. is recalling 26 boxes of Buttermilk Ranch Snack Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
Copperleaf Kitchen is recalling Country Gardens Cuisine Broccoli Cheese Soup with Rice after a supplier reported positive environmental tests for Salmonella.
All American Seasonings is recalling 428 bags of Non-GMO Sour Cream & Onion seasoning due to potential Salmonella contamination.
All American Seasonings is recalling 80 bags of Kay's Naturals Cheese Puff Seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canada.
All American Seasonings, Inc. is recalling 211 bags of 50 lb Spicy Nacho seasoning due to potential Salmonella contamination. The product was distributed nationwide and to Canadian consignees.
Thor Motor Coach is recalling 2017 Aria motorhomes because the driver's side sofa seatbelts may be too short for passengers to use.
Stryker Sustainability Solutions is recalling reprocessed electrophysiology catheter cables because a breach in sterile packaging may have occurred, potentially rendering the product non-sterile.
Elekta, Inc. is recalling Oncentra External Beam and Brachy software because a cross profile for a Varian 60-degree wedge shows 'horns.' The recall covers 433 units distributed worldwide.
Noven Pharmaceuticals is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed to meet mechanical peel force specifications.
Williams-Sonoma is recalling Meyer Lemon Poppy Quick Bread Mix because it was made with milk powder linked to a Salmonella recall.
C.R. Bard is recalling specific medical device trays and stabilization devices because they contained latex catheters instead of silicone catheters.
Philips is recalling 35 IQon Spectral CT systems due to software issues causing rescans, incorrect scan locations, or misrepresentation of image results.
Brand Castle LLC is recalling In The Mix Monkey Bread Mix because the facility and finished product tested positive for Salmonella.
Medtronic Navigation is voluntarily recalling 111 AxIEM Touch N Go Pointer Probes because they may compromise navigation accuracy during patient registration.
Beckman Coulter is recalling the DxH 600 Cellular Analysis System because it may fail to detect blasts in some blood samples.
Siemens is recalling Artis Q angiographic x-ray systems due to potential high-voltage generator failures and rare image display loss.
ICU Medical is recalling Tego Connectors due to a potential risk of leaking. The devices are used as accessories for vascular access in hemodialysis.
Stryker is recalling reprocessed ablation catheter cables because a breach in sterile packaging may have resulted in non-sterile product.
Philips is recalling 41 Clinix RF Plus X-ray systems because liquid penetration can cause an unintentional tilt of the diagnostic table.
Nissan is recalling 2015-2017 Altima vehicles because improperly routed rear door latch cables may allow doors to open while driving, increasing injury risk.
Beckman Coulter is recalling the UniCel DxH 800 Cellular Analysis System because it may fail to detect blasts in some blood samples.
Forest River is recalling 2017 Prime Time Avenger recreational vehicles because incorrect Federal Placards may lead to tire over-inflation and blowouts.