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. 2,295 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,295 in last 12 months

Showing 4134141360 of 47,632 recalls

DrugDecember 4, 2013· Teva Pharmaceuticals USA

Recalled Item: Qnasl (beclomethasone dipropionate) Nasal Aerosol Recalled by Teva...

The Issue: Defective Delivery System: There is a potential for some units in certain...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 4, 2013· Invivo Corporation

Recalled Item: Invivo Corporation Expression Information Portal (Model IP5) is intended to...

The Issue: Invivo Corporation located at 12151 Research Parkway, Orlando, FL 32826 is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Sorin Group Deutschland GmbH

Recalled Item: S5/C5 Heart-lung machine Product Usage: The StOckert S5/ Sorin C5 Recalled...

The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Sorin Group Deutschland GmbH

Recalled Item: CP5 centrifugal pump system Product Usage: The Stockert S5/ Sorin Recalled...

The Issue: Sorin is initiating a field correction on S5/C5 Heart-lung machine and CP5...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: ADAC ARGUS Gamma Camera Systems & ADAC CIRRUS Gamma Camera Recalled by...

The Issue: The recalling firm determined that visual inspections of the fork joints...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2013· Philips Medical Systems (Cleveland) Inc

Recalled Item: Computed Tomography X-Ray System (Brilliance CT Big Bore Oncology & Recalled...

The Issue: Machine Name in TumorLOC Basic Mode is obscured. When TumorLOC is in Basic...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2013· The Anspach Effort, Inc.

Recalled Item: Anspach Irrigation Clip 40 Product Usage: Irrigation clips provide a...

The Issue: The Irrigation Clips were assembled with the incorrect (smaller) clips.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2013· Baxter Corporation Englewood

Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...

The Issue: Baxter Healthcare Corporation is issuing a voluntary correction for ABACUS...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2013· Microgenics Corporation

Recalled Item: MAS Omni Immune PRO Controls Recalled by Microgenics Corporation Due to The...

The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...

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

Class III — Low RiskOngoing
Medical DeviceDecember 2, 2013· Microgenics Corporation

Recalled Item: MAS Omni Immune Controls Recalled by Microgenics Corporation Due to The...

The Issue: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni...

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

Class III — Low RiskOngoing
Medical DeviceNovember 29, 2013· EOS Imaging

Recalled Item: steroEOS Workstation with software versions: 1.3 Recalled by EOS Imaging Due...

The Issue: Error copying information to the clinical file and to the report when two 3D...

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

Class II — Potential Health HazardOngoing
DrugNovember 27, 2013· Wockhardt Usa Inc.

Recalled Item: Pantaprazole Sodium Delayed Release Tablets Recalled by Wockhardt Usa Inc....

The Issue: Failed Dissolution Specifications; 12 month acid dissolution test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 27, 2013· B. Braun Medical Inc

Recalled Item: 0.45% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Labeling: Wrong Bar Code; Bar code scans as 0.15% Potassium Chloride in 0.9%...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 27, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE has become aware of...

The Issue: GE has become aware of multiple issues affecting the Dash 3000/4000/5000...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2013· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module The Patient Data Module Recalled...

The Issue: GE Healthcare has recently become aware of a potential safety issue due to...

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

Class II — Potential Health HazardOngoing
DrugNovember 26, 2013· Humco Holding Group, Inc

Recalled Item: Mercuroclear Antiseptic Anesthetic First Aid Helps prevent infection and...

The Issue: Microbial Contamination of Non-Sterile Product(s): The product was found to...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 26, 2013· Teva Pharmaceuticals USA

Recalled Item: Niacin Extended Release Tablets Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Tablet/Capsule Specifications: There is a potential for broken tablets.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 26, 2013· Orthofix, Inc.

Recalled Item: Orthofix Firebird Spinal Fixation System Instrumentation Modular Screw...

The Issue: Orthofix received 6 complaints which resulted in a reportable events due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2013· Becton Dickinson & Company

Recalled Item: BD Interlink threaded lock cannula This is a locking blunt Recalled by...

The Issue: BD Interlink Threaded Lock Cannula REF# 303369 and lot #3021392 is being...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2013· Stryker Medical Division of Stryker Corporation

Recalled Item: Secure II Med/Surg Bed Secure II and the 3002 S3 Recalled by Stryker Medical...

The Issue: Stryker Medical has identified a potential issue associated with Secure II...

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

Class II — Potential Health HazardOngoing