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. 983 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
983 in last 12 months

Showing 30301–30320 of 50,117 recalls

Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Recalled by Breg Inc Due to They may not have been sealed prior to...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Back Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Shldr Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Rect L Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: If Hip Recalled by Breg Inc Due to They may not have been sealed prior to...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
DrugMarch 30, 2017· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID) Recalled by Bayer...

The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2017· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Alka-Seltzer Gold (1000 mg Anhydrous citric acid Recalled by Bayer...

The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 30, 2017· Bayer HealthCare Pharmaceuticals, Inc.

Recalled Item: Alka-Seltzer Original ( 325 mg Aspirin (NSAID) Recalled by Bayer HealthCare...

The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 30, 2017· Barco N.V.

Recalled Item: Optional MDRC-1119 Front Cover Attachment Kit for review display monitors....

The Issue: If metal strips are removed and re-applied to another display, there is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2017· Teleflex Medical

Recalled Item: Arrow EZ-IO Needle Set 45 mm 15 ga Recalled by Teleflex Medical Due to Some...

The Issue: Some of the individual unit packaging (pouches) may be missing the lot...

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

Class III — Low RiskOngoing
Medical DeviceMarch 29, 2017· Stryker Medical Division of Stryker Corporation

Recalled Item: Medi-Therm Hyper/Hypothermia System Recalled by Stryker Medical Division of...

The Issue: The water may reheat too quickly if the unit is in "Automatic" mode,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GP321R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing