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. 2,365 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,365 in last 12 months

Showing 2450124520 of 27,558 recalls

Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 2 Recalled by Ortho-Clinical...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Zimmer, Inc.

Recalled Item: Trabecular Metal" Reverse Shoulder System Recalled by Zimmer, Inc. Due to As...

The Issue: As a result of complaints for disassociation of the TM Reverse Glenosphere...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Baxter Healthcare Corp

Recalled Item: 15 L Cycler Drainage Bag Product Usage: For use with Recalled by Baxter...

The Issue: The large tube clamp used to close the drain tube on the 15 L Cycler...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 17, 2013· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Na+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Ortho Clinical Diagnostics has recalled VITROS Chemistry Products Na+ Slides...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Bausch & Lomb Surgical, Inc.

Recalled Item: Bausch & Lomb AKREOS AO Micro Incision Lens The Akreos Recalled by Bausch &...

The Issue: Lens was manufactured with incorrect raw material.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Cutera, Inc.

Recalled Item: Cutera brand truSculpt infrared System (optional) Recalled by Cutera, Inc....

The Issue: Cutera received two adverse events associated with the edge of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 16, 2013· Baxter Healthcare Corp.

Recalled Item: The HomeChoice Pro APD System is a peritoneal dialysis system. Recalled by...

The Issue: The occluder in affected devices 1) may have sharp edges that could cut the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Teleflex Medical

Recalled Item: Green Rusch - Lite Disposable Metal Laryngoscope Ridge Blade to Recalled by...

The Issue: Labeling inconsistency

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 15, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Material Mix (Adjustable Cervical Distractor-Right Recalled by...

The Issue: One material batch used for production of the affected parts of the Synthes...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Healthcare Informatics, Inc.

Recalled Item: Philips brand IntelliSpace PACS 4.4 Recalled by Philips Healthcare...

The Issue: Philips Healthcare became aware of a software problem with the IntelliSpace...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Fresenius Medical Care Holdings, Inc.

Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...

The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Synthes (USA) Products LLC

Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...

The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 14, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....

The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2013· Restoration Robotics

Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...

The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: 3.5 X 10 CORT SCREW SELFT 3.5 X 12 CORT Recalled by Zimmer, Inc. Due to...

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 11, 2013· Zimmer, Inc.

Recalled Item: TRILOGY ACET SHELL 36MM O TRILOGY ACET SHELL 38MM O Recalled by Zimmer, Inc....

The Issue: Zimmer recently conducted a review of all historic packaging validations at...

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

Class II — Potential Health HazardOngoing