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. 2,527 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,527 in last 12 months

Showing 1674116760 of 50,117 recalls

Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: RINGLOC BIPOLAR Hip System Bi Polar Locking Ring Recalled by Biomet, Inc....

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2020· Biomet, Inc.

Recalled Item: Comprehensive Reverse Shoulder System Recalled by Biomet, Inc. Due to...

The Issue: Specific lots of multiple sterile medical devices may have a breach in the...

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

Class II — Potential Health HazardOngoing
DrugNovember 25, 2020· US Compounding Inc

Recalled Item: Neostigmine Methylsulfate PF Inj. 5 mg/5 mL Recalled by US Compounding Inc...

The Issue: Labelling: Missing label.

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2020· Torrent Pharma Inc

Recalled Item: Anagrelide Capsules Recalled by Torrent Pharma Inc Due to Failed Dissolution...

The Issue: Failed Dissolution Specifications

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 24, 2020· Siemens Medical Solutions USA, Inc

Recalled Item: SOMATOM Force Recalled by Siemens Medical Solutions USA, Inc Due to System...

The Issue: System does not trigger a cancel command followed by a reload of the scan...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Tuohy-Borst Side-Arm Introducer (Shuttle Select) Recalled by Cook...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Tuohy-Borst Side-Arm Introducer (Shuttle Select) Recalled by Cook...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 24, 2020· Cook Inc.

Recalled Item: Flexor Check-Flo Introducer Recalled by Cook Inc. Due to There is an...

The Issue: There is an increased likelihood of the introducer sheath separating at the...

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

Class I — Serious Health HazardOngoing