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. 1,854 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,854 in last 12 months

Showing 2382123840 of 28,538 recalls

Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit Recalled by...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit Recalled by...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2014· Navilyst Medical, Inc

Recalled Item: PICC Convenience Kit with Accessories Recalled by Navilyst Medical, Inc Due...

The Issue: NMI was notified by the manufacturer of the 10 ml BD PosiFlush SF Saline...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2014· DeRoyal Industries Inc

Recalled Item: Suction canisters labels as follows: 1) DeRoyal(R) SUCTION CANISTER Recalled...

The Issue: These lots of suction canisters and lids have an insufficient seal under low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2014· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) SafeLiner Suction Canister Kit Recalled by DeRoyal Industries Inc...

The Issue: These lots of suction canisters and lids have an insufficient seal under low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2014· Beckman Coulter Inc.

Recalled Item: UniCel 600/800 Access Immunoassay Systems are in vitro diagnostic devices...

The Issue: Beckman Coulter is recalling the Sample Probe Cable because nonconforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2014· Maquet Medical Systems USA

Recalled Item: TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Recalled by...

The Issue: The wrong movement results on the MAGNUS OR table. The button commands on...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 21, 2014· Philips Medical Systems, Inc.

Recalled Item: Ingenia Recalled by Philips Medical Systems, Inc. Due to When a fused series...

The Issue: When a fused series of a sagittal, coronal or radial multi station scan is...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 20, 2014· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products PHYT (Phenytoin) Slides Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics identified a potential for biased results to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: 83" (211 cm) Appx 10.3 mL Recalled by ICU Medical, Inc. Due to ICU is...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· St Jude Medical Cardiac Rhythm Management Division

Recalled Item: Ellipse Implantable Cardioverter Defibrillators (ICDs) Recalled by St Jude...

The Issue: An anomaly may result in delayed, partial, or no delivery of high voltage...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens CentraLink Data Management System Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has identified a task scheduler issue with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: 98" (249 cm) Appx 12.3 ml Recalled by ICU Medical, Inc. Due to ICU is...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 19, 2014· ICU Medical, Inc.

Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...

The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 18, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Siemens Dimension Vista¿ CHEM 1 CAL Recalled by Siemens Healthcare...

The Issue: Siemens Healthcare Diagnostics has received complaints for low recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 18, 2014· Elekta, Inc.

Recalled Item: FOCAL Sim Workstation Recalled by Elekta, Inc. Due to When DICOM is...

The Issue: When DICOM is exporting an arc plan (VMAT, Dynamic Conformal of 3D Static...

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

Class II — Potential Health HazardOngoing