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. 2,594 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,594 in last 12 months

Showing 94819500 of 50,117 recalls

FoodApril 18, 2023· Country Cookie LLC.

Recalled Item: Country Cookie Oatmeal Scotchie cookie Recalled by Country Cookie LLC. Due...

The Issue: Allergen contains statement does not declare "Milk"

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 18, 2023· Olympus Corporation of the Americas

Recalled Item: Olympus Single Use Distal Cover Model Number MAJ-2315 used with Recalled by...

The Issue: The Single Use Distal Cover MAJ-2315 may cause mucosal injury and/or become...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2023· DeRoyal Industries Inc

Recalled Item: Sterile custom surgical procedure packs (1) 89-10529.04 Recalled by DeRoyal...

The Issue: The custom procedure packs contain light handle covers that have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2023· DeRoyal Industries Inc

Recalled Item: Sterile custom surgical procedure packs: (1) 89-10507.02 Recalled by DeRoyal...

The Issue: The custom procedure packs contain light handle covers that have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products HbA1c Reagent Kit- IVD for the quantitative...

The Issue: Potential for both unexpected positive and negative HbA1c results, may...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P)180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Set2Go Ventilation 12 (A) Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Seattle PAP Plus Recalled by Draeger Medical, Inc. Due to Glued connections...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia WT (P)180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Set Coax 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Abiomed, Inc.

Recalled Item: Impella 5.5 with SmartAssist catheter is an intravascular micro axial...

The Issue: The Impella 5.5 pump experienced a heightened complaint rate for purge leaks.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Anesthesia (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax Recalled by Draeger Medical, Inc. Due to Glued connections of...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: ID Circuit Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P)250 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax 3 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax 1 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing