Product Recalls in South Dakota

Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,386 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,386 in last 12 months

Showing 2218122200 of 27,558 recalls

Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray systems Brilliance iCT Recalled by Philips Medical...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity CT scanners. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Brilliance iCT SP. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-ray Systems Ingenuity Core 128. Intended to produce...

The Issue: 5 issues. Fast Get Ready incorrectly enabled during service procedures....

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 16 Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8i Surgical Skin Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Arrow International Inc

Recalled Item: ARROW FiberOptix Intra-Aortic Balloon Catheter Kit Recalled by Arrow...

The Issue: Outer package product label incorrectly identifies the product as FiberOptix...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Zipline Medical

Recalled Item: Zip 8M Wound Closure Device Recalled by Zipline Medical Due to The...

The Issue: The manufacturers seal may not be present on the Nylon pouch resulting in...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2015· Derma Pen, LLC

Recalled Item: DermaPen Pro Model Recalled by Derma Pen, LLC Due to Derma Pen initiated a...

The Issue: Derma Pen initiated a field communication for Dermapen after receiving an...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2015· Fujifilm Medical Systems U.S.A., Inc.

Recalled Item: Fujifilm Synapse Cardiovascular I ProSolv CardioVascular Synapse...

The Issue: Under certain circumstances the patient Demographics in a report exported...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS vascular System Model : 722122 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper cardio systems Model : 722123 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Norwex Usa Inc

Recalled Item: Manual Toothbrush Recalled by Norwex Usa Inc Due to The toothbrush head can...

The Issue: The toothbrush head can potentially disengage from the handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Allura Xper Series: Allura Xper FD10 Allura Xper Recalled...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Allure BiPlane Series: Model 722013 Allura Xper FD20...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Synthes, Inc.

Recalled Item: Synthes Inserter for Titanium Elastic Nails Recalled by Synthes, Inc. Due to...

The Issue: The Inserter has the potential for mechanical failures such as breakage of...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare INTEGRIS cardio system Model : 722121 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper vascular system Model : 722124 Product Usage:...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2015· Philips Medical Systems, Inc.

Recalled Item: Philips Healthcare Xper vascular systems R7.6 Model : 722134 Product...

The Issue: Monitor Ceiling Suspension system may fall

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

Class II — Potential Health HazardOngoing