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. 2,636 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,636 in last 12 months

Showing 22012220 of 50,117 recalls

Medical DeviceJune 4, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN2 Control) Recalled by...

The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (Norm Control) Recalled by...

The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ 120/2120/2120i 3-in-1 TESTpoint Control (ABN1 Control) Recalled by...

The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2025· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA¿ 120/2120/2120i SETpoint Calibrator Recalled by Siemens Healthcare...

The Issue: Products have the incorrect platelet (PLT) value assignments for the ADVIA...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: UROSKOP Omnia. Model Number: 10094910 Recalled by Siemens Medical Solutions...

The Issue: A resistor in the frequency inverter may strongly overheat potentially...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 4, 2025· Siemens Medical Solutions USA, Inc

Recalled Item: UROSKOP Omnia Max. Model Number: 10762473 Recalled by Siemens Medical...

The Issue: A resistor in the frequency inverter may strongly overheat potentially...

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

Class II — Potential Health HazardOngoing
FoodJune 3, 2025· Peak Cocktails

Recalled Item: Peak Cocktails Blood Orange Spritz 8.4 fl oz aluminum cans Recalled by Peak...

The Issue: Overpressurization leading to exploding cans

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 3, 2025· Hamilton Medical AG

Recalled Item: Hamilton C6 (ESM Board PN 10144626 UDI-DI code: Recalled by Hamilton Medical...

The Issue: A mechanical defect on a printed circuit board (PCB) as a result of PCB...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2025· ICU Medical, Inc.

Recalled Item: SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve Recalled by...

The Issue: Due to a manufacturing issue, disinfecting cap for needle-free connectors...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2025· Given Imaging Ltd.

Recalled Item: Bravo CF capsule delivery device Recalled by Given Imaging Ltd. Due to It...

The Issue: It has been determined that misapplied adhesive on the Bravo CF capsule...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 3, 2025· C.R. Bard Inc

Recalled Item: Recalled by C.R. Bard Inc Due to Cather packaging may contain the incorrect...

The Issue: Cather packaging may contain the incorrect French size.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2025· C.R. Bard Inc

Recalled Item: BD Heyman Follower Straight Tip for following sizes: 10Fr - Recalled by C.R....

The Issue: Cather packaging may contain the incorrect French size.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 3, 2025· C.R. Bard Inc

Recalled Item: BD Heyman Follower Coude Tip for following sizes: 12Fr - Recalled by C.R....

The Issue: Cather packaging may contain the incorrect French size.

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

Class II — Potential Health HazardOngoing
FoodJune 2, 2025· La Fontanella Food Products LLC

Recalled Item: Pizza Shoppe The "Pink Stuff" World-Famous Creamy Garlic Salad Dressing...

The Issue: Potential for product spoilage (increased level of lactic acid detected in...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: KETAmine Hydrochloride Injection Recalled by Tailstorm Health INC Due to...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: LIDOcaine HCL Sterile Injection Recalled by Tailstorm Health INC Due to Lack...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: KETAmine Hydrochloride Injection Recalled by Tailstorm Health INC Due to...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: BUPIVAcaine HCL Sterile injection Recalled by Tailstorm Health INC Due to...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: LIDOcaine HCl Injection Recalled by Tailstorm Health INC Due to Lack of...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 2, 2025· Tailstorm Health INC

Recalled Item: LIDOcaine HCL Sterile Injection Recalled by Tailstorm Health INC Due to Lack...

The Issue: Lack of Assurance of Sterility: A recent FDA inspection revealed concerns...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund