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. 2,452 recalls have been distributed to South Dakota in the last 12 months.

47,632 total recalls
2,452 in last 12 months

Showing 1590115920 of 27,558 recalls

Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Philips Medical Systems Nederlands

Recalled Item: MultiDim Eleva 708032 As a multifunctional universal imaging application...

The Issue: The fixation of the upper and lower tilt actuator, of the MD-Eleva system...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire Bullet Tip 2.4 mm Diameter...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Humeral Guide Wire Ball Tip 2.4 mm Diameter 70 cm Length Recalled by Zimmer...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW Recalled by...

The Issue: Slot screw had an overall length of 15mm, but per the specification, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Medtronic Navigation, Inc.

Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part...

The Issue: Medtronic has become aware that certain lots of the VCLAS 3MM, 10MM, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 015 Recalled by Straumann Manufacturing, Inc. Due to A...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack USA. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E90 ultrasound system Product Usage: Vivid E80 / Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Lithium Heparin Green Top Tube Recalled by Becton Dickinson &...

The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E80 ultrasound system Vivid E80 / E90 / Recalled by GE Medical...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E9 ultrasound system Product Usage: GE Vivid E9 Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE LOGIQ 9 ultrasound system Product Usage: The device is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ EDTA Tan Top Tube Recalled by Becton Dickinson & Company Due...

The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...

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

Class I — Serious Health HazardOngoing