Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,404 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,404 in last 12 months

Showing 3530135320 of 50,117 recalls

Medical DeviceJanuary 8, 2016· DePuy Orthopaedics, Inc.

Recalled Item: SIGMA HP MBT Non-Keel Punch Knee Instrument. Designed to be Recalled by...

The Issue: Increased punch height, causing a 0.063 in (1.6 mm) gap between the trial...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2016· Natus Medical Incorporated

Recalled Item: Medix NatalCare ST-LX Intensive Care Incubator. Neonatal incubator. Recalled...

The Issue: NatalCare LX Incubators were manufactured using a defective oval port hinge...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2016· Olympus Corporation of the Americas

Recalled Item: Olympus TJF-Q180V flexible gastrointestinal Duodenoscope Product Usage: This...

The Issue: Olympus America Inc is conducting a voluntary removal/corrective action of...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodJanuary 8, 2016· Good Earth Egg Company

Recalled Item: Shell eggs Recalled by Good Earth Egg Company Due to Potential Salmonella...

The Issue: May be contaminated with Salmonella.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 7, 2016· Madison One Acme Inc

Recalled Item: Tong Ren Tang Shenjing Shuairuo Wan Herbal Supplement 240 pills Recalled by...

The Issue: Madison One Acme, Inc. dba Solstice Medicine is recalling Tong Ren Tang...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2016· Heartware, Inc.

Recalled Item: HeartWare Ventricular Assist System: HeartWare Battery Recalled by...

The Issue: Heartware Ventricular Assist System Battery Cell experiencing premature...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 7, 2016· Wfr/aquaplast Corp

Recalled Item: Clear Vue Prone Breast Treatment Table and Access ClearVision Prone Recalled...

The Issue: Some of the Access ClearVue Prone Breast devices may contain scales that are...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Femoral Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Central Venous Catheter Sets and Trays The subject Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Radial Artery Pressure Monitoring Catheter Sets and Trays The subject...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2016· Cook Inc.

Recalled Item: Single Lumen Pressure Monitoring Sets and Trays The subject sets Recalled by...

The Issue: A manufacturing process may lead to catheter tip fracture and or separation....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 6, 2016· Zimmer Dental Inc

Recalled Item: IMPLANT Recalled by Zimmer Dental Inc Due to Information specific to the 3.7...

The Issue: Information specific to the 3.7 mmD and 4.1 mmD Trabecular Metal Zimmer...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing