State

Kansas product recalls

73,824 recalls have nationwide distribution and so reach Kansas. 5,822 additional recalls listed Kansas specifically in their distribution scope.

What the numbers show

Total: 5,822
Critical: 1,053
Severe: 1,486
Most recent: 2026-11-04

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.

48126–48150 of 79646

SevereFDA (Food)·F-1491-2017·2017-03-01
Hy-Vee Peppermint Bark Recalled Due to Potential Salmonella Contamination
Hy-Vee Stores Inc is recalling Peppermint Bark products because an ingredient may be contaminated with Salmonella. The recall affects specific retail stores in eight states.
Product
Peppermint Bark packaged in 4oz. (UPC 026133800000),12 oz. (UPC 026133700000) plastic tray containers, and 9 oz. tubs (UPC 026267900000) for retail sale, labeled with Hy-Vee scale ticket. The product was labeled HyVee West Des Moines, IA.
Category
Food
Distribution
8 states
SevereFDA (Devices)·Z-1164-2017·2017-03-01
Biomet Recalls Oxford Partial Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
SevereFDA (Drugs)·D-0480-2017·2017-03-01
Hospira Recalls Metronidazole Injection Bags Due to Leaking
Hospira is recalling 578,784 bags of Metronidazole Injection due to a customer report of a leaking bag, which compromises sterility assurance.
Product
METRONIDazole Injection, USP 500 mg (5 mg/mL) in 100 mL Single Dose Flexible Container, Rx only, For IV Use, Hospira Inc., Lake Forest, IL --- NDC 0409-7811-24
Category
Drug
Distribution
Distributed nationwide
SevereUSDA FSIS·019-2017·2017-03-01
Dos Hermanos Recalls Beef Jerky Produced Without Federal Inspection
Dos Hermanos, Inc. is recalling approximately 151 pounds of Carne Seca Beef Jerky produced without federal inspection. The products were distributed in Illinois, Iowa, Kansas, and Missouri.
Product
Dos Hermanos, Inc. Recalls Beef Jerky Products Produced Without Benefit of Inspection
Category
Food
Distribution
4 states
HighFDA (Devices)·Z-1161-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1172-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1225-2017·2017-03-01
Tosoh HLC-723G8 Analyzer Recalled for HbA1c Test Inaccuracy
Tosoh Bioscience is recalling 682 HLC-723G8 analyzers because they may report inaccurate HbA1c values for patients with specific hemoglobin variants.
Product
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Category
Medical Device
Distribution
49 states
HighFDA (Devices)·Z-1174-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Left Medial Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighCPSC·17097·2017-03-01
Pier 1 Imports Recalls Glass Knobs Due to Laceration Hazard
Pier 1 Imports is recalling about 363,000 glass knobs sold in the U.S. because they can break and cause lacerations.
Product
Glass knobs
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1157-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size F Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1228-2017·2017-03-01
Arrow International Recalls Vascular Catheter Introduction Kits Due to Flaring Sheaths
Arrow International Inc is recalling 215,703 vascular catheter introduction kits nationwide because complaints were received regarding peel away sheaths flaring.
Product
Vascular catheter introduction kit The PICC is indicated for short or long term peripheral access to the central Venous system for intravenous therapy, blood sampling, infusion and power injection of contrast media.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1152-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee System Tibial Resector Body Tubes and Guides due to potential alumina inclusions that could cause the instruments to crack or separate.
Product
Oxford Knee System Tibial Resector Body Tube & Guides Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1173-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Potential Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Phase 3 Tibial Template Right Medial Size C Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1159-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Left Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Food)·F-1527-2017·2017-03-01
Falafel King Recalls Tzatziki Sauce for Undeclared Milk Allergen
Falafel King is recalling 1,380 containers of Tzatziki Sauce due to undeclared milk on the label. The product was distributed in Colorado, New Mexico, Utah, and Nebraska.
Product
Falafel King Tzatziki Sauce. 10 ounce. Plastic container
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1170-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 1 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 1 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1158-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size A Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighNHTSA·17V127000·2017-03-01
Volvo Recalls 2017 Models for Side Air Bag Inflator Defect
Volvo is recalling 2017 S60, V60, and XC60 vehicles because side air bag inflators may fail to ignite, preventing deployment in a crash.
Product
VOLVO — VOLVO V60, XC60, S60, V60CC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1169-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 2 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1154-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Tibial Impactor Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1162-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size D Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1160-2017·2017-03-01
Biomet Oxford Knee Instruments Recalled for Material Inclusions
Biomet is recalling Oxford Partial Knee instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size E Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighNHTSA·17V129000·2017-03-01
Forest River Recalls 2017 Rockwood and Flagstaff Trailers for Tire Defect
Forest River is recalling 2017 Rockwood and Flagstaff recreational trailers because a slide room bracket may damage the front tire, causing deflation and increasing crash risk.
Product
FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1166-2017·2017-03-01
Biomet Oxford Partial Knee Instruments Recalled for Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Partial Knee System instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Partial Knee System Right Medial Tibial Trial Tray Size B Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states
HighFDA (Devices)·Z-1168-2017·2017-03-01
Biomet Recalls Oxford Knee Instruments Due to Material Inclusions
Biomet U.K., Ltd. is recalling Oxford Unicompartmental Knee Phase 3 Shim Size 3 instruments due to potential alumina inclusions that could cause cracking and separation.
Product
Oxford Unicompartmental Knee Phase 3 Shim Size 3 Product Usage: Instruments for use with the Oxford Uni Partial Knee System
Category
Medical Device
Distribution
14 states