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. 2,573 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
2,573 in last 12 months

Showing 1072110740 of 28,538 recalls

Medical DeviceNovember 10, 2020· Baxter Healthcare Corporation

Recalled Item: MiniCap Extended Life PD Transfer Set Recalled by Baxter Healthcare...

The Issue: Potential for no-flow and leaks under the twist clamp.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· CryoLife, Inc.

Recalled Item: CryoValve SG Pulmonary Human Heart Valve. The valve is cryopreserved...

The Issue: On November 10, 2020, it was discovered that there are post- processing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Slim Recalled by TissueTech, Inc. Due to Potential exposure of...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Recalled by TissueTech, Inc. Due to Potential exposure of product to...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· CryoLife, Inc.

Recalled Item: CryoPatch SG Pulmonary Human Cardiac Patch. The patch is cryopreserved...

The Issue: On November 10, 2020, it was discovered that there are post- processing...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· TissueTech, Inc.

Recalled Item: PROKERA Plus Recalled by TissueTech, Inc. Due to Potential exposure of...

The Issue: Potential exposure of product to microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 10, 2020· Applied Medical Technology Inc

Recalled Item: AMT Male ENFit-to-Stepped Male (Christmas Tree) Adapter Recalled by Applied...

The Issue: The products subject to this recall may contain obvious, incorrect pouch...

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

Class III — Low RiskOngoing
Medical DeviceNovember 9, 2020· Exactech, Inc.

Recalled Item: Equinoxe Humeral Stem Recalled by Exactech, Inc. Due to Potential for...

The Issue: Potential for incorrect Instructions For Use (IFU) included with an Equinoxe...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· Shimadzu Medical Systems

Recalled Item: Shimadzu Mobile X-Ray System Recalled by Shimadzu Medical Systems Due to...

The Issue: There is a potential that the adjustable handle option on the X-Ray system...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· ICU Medical, Inc.

Recalled Item: icumedical Cogent" Hemodynamic Monitoring System - Product Usage: intended...

The Issue: Due to a potential software issue, the display may show the incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· Helena Laboratories, Corp.

Recalled Item: K-ACT Actalyke Clotting Test Tubes that are used in the: Recalled by Helena...

The Issue: Due to complaints received associated with cracked/split test tube caps.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 9, 2020· Canon Medical System, USA, INC.

Recalled Item: Canon Aquilion Prime SP Recalled by Canon Medical System, USA, INC. Due to A...

The Issue: A software problem has been identified which could result in the CT Scanner...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Bausch & Lomb Surgical, Inc.

Recalled Item: MX60ET (enhanced enVista Toric) enVista¿ One-Piece Hydrophobic Acrylic Toric...

The Issue: Product may be missing toric axis marks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate bottles Recalled by Fresenius Medical...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 7, 2020· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte Liquid Acid concentrate drums Recalled by Fresenius Medical Care...

The Issue: The sodium and/or calcium levels in these concentrates were below the...

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

Class II — Potential Health HazardOngoing