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. 2,423 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,423 in last 12 months

Showing 2614126160 of 50,117 recalls

Medical DeviceMay 3, 2018· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: CARDIOSAVE Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Maquet...

The Issue: Ingress of fluids into the device can affect various electronic circuit...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 3, 2018· Joerns Healthcare

Recalled Item: ProCair Mattress: (a) PROCAIR PLUS 42X80 Recalled by Joerns Healthcare Due...

The Issue: Joerns Healthcare has identified a potential issue with some of the P.R.O....

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: NaturaLyte¿ Liquid Acid Concentrate for Bicarbonate Dialysis Recalled by...

The Issue: The bottles are mislabeled with an incorrect part number.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Roche Molecular Systems, Inc.

Recalled Item: MagNA Pure 24 System Recalled by Roche Molecular Systems, Inc. Due to...

The Issue: Cross-contamination of samples has been reported when running the existing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Heartware

Recalled Item: Heartware Medtronic HVAD System for cardiac use. Including the following...

The Issue: Possible transient electrical connection interruption between an HVAD System...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 2, 2018· Smith & Nephew, Inc.

Recalled Item: smith&nephew ANTHOLOGY POROUS HIGH OFFSET STEM Recalled by Smith & Nephew,...

The Issue: Three lots of Anthology HO Porous size 7 stems were manufactured with an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2018· Ad-Tech Medical Instrument Corporation

Recalled Item: AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N...

The Issue: The diameter of the drill sleeve guide raw material was found to be under...

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

Class II — Potential Health HazardOngoing
FoodMay 2, 2018· Badger Botanicals LLC

Recalled Item: Acadica Kratom: Green Hulu 2 Kratom Recalled by Badger Botanicals LLC Due to...

The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2018· Badger Botanicals LLC

Recalled Item: Acadica Kratom: Green Suma Recalled by Badger Botanicals LLC Due to...

The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2018· Badger Botanicals LLC

Recalled Item: Acadica Kratom: Red Suma 250g bags Recalled by Badger Botanicals LLC Due to...

The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2018· Badger Botanicals LLC

Recalled Item: Acadica Kratom: Red Hulu 2 Recalled by Badger Botanicals LLC Due to...

The Issue: Recalling Red Suma, Green Suma, Red Hulu 2, Green Hulu 2 Kratom products due...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 1, 2018· Hobbs Medical, Inc.

Recalled Item: Hobbs Bronchial Cytology Brushes Recalled by Hobbs Medical, Inc. Due to...

The Issue: Device was marketed for uses outside the 510(k) clearance.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q.zen biplane Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee floor MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee MP Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to After the...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q biplane Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee biplane MN Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 1, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis Q ceiling Recalled by Siemens Medical Solutions USA, Inc Due to After...

The Issue: After the Large Display returns from power save mode, it may not show an...

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

Class II — Potential Health HazardOngoing