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. 2,476 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,476 in last 12 months

Showing 1936119380 of 50,117 recalls

Medical DeviceJanuary 9, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Single-Use Metal Laryngoscope Blade for Fiber Optic System...

The Issue: The products are being recalled due to reports of breakage broke at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Uroskop Omnia max Model: 10762473 - Product Usage:...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Ysio Max - Interventional Fluoroscopic X-Ray System...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos Agile Max Model: 10762472 - Product Usage:...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Healthineers Luminos dRF Max Model: 10762471- Product Usage: is...

The Issue: Two software issues (1) Using the override function in case of blocked...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to A software...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A software bug may lead to one image to be assigned to two different...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 8, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: Uroskop Omnia max Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Siemens became aware of an issue of incorrect use of the bypass key...

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

Class II — Potential Health HazardOngoing
DrugJanuary 7, 2020· AVKARE Inc.

Recalled Item: Dutasteride Capsules Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: High out of specification...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2020· Golden State Foods

Recalled Item: Garlic Parmesan Sauce Recalled by Golden State Foods Due to Notification by...

The Issue: Notification by supplier of a recall of starch ingredient due to metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2020· Golden State Foods

Recalled Item: Taco Bell Creamy Jalapeno Sauce Recalled by Golden State Foods Due to...

The Issue: Notification by supplier of a recall of starch ingredient due to metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2020· Golden State Foods

Recalled Item: Pizza Hut Garlic Dipping Sauce Recalled by Golden State Foods Due to...

The Issue: Notification by supplier of a recall of starch ingredient due to metal...

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

Class II — Potential Health HazardOngoing
Refund
FoodJanuary 7, 2020· Golden State Foods

Recalled Item: Colonel's Coleslaw Dressing Recalled by Golden State Foods Due to...

The Issue: Notification by supplier of a recall of starch ingredient due to metal...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 7, 2020· Stryker Corporation

Recalled Item: Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only Recalled by...

The Issue: Sterile drapes packaged in an unsealed pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Stryker Corporation

Recalled Item: Spy-Phi Drape only (HH2020) Pack of 20 HH2000 (Sold internationally Recalled...

The Issue: Sterile drapes packaged in an unsealed pouch.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Smiths Medical ASD, Inc.

Recalled Item: Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin Recalled...

The Issue: Lots of Smiths Medical Portex Pro-Vent and LineDraw Arterial Blood Sampling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 7, 2020· Smiths Medical ASD, Inc.

Recalled Item: Portex LineDraw Arterial Blood Sampling Syringe with Dry Lithium Heparin...

The Issue: Portex Pro-Vent and LineDraw Arterial Blood Sampling syringes may have...

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

Class II — Potential Health HazardOngoing