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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 26941–26960 of 47,632 recalls
Recalled Item: IQF Green Beans Recalled by Lakeside Foods, Inc Due to Potential Listeria...
The Issue: IQF French Style Green Beans and IQF Cut Green Beans may be contaminated...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic Synchromed II Model 8637 supplied in 20mL and 40 Recalled by...
The Issue: Medtronic implemented a final design change intended to address the motor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Module model 8100 manufactured between November 2011 and March...
The Issue: The recalling firm has received reports of increased or decreased flows that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REVOLVE ADVANCED ADIPOSE SYSTEM Recalled by LifeCell Corporation, A Wholly...
The Issue: Presence of bacterial endotoxins levels above the acceptable limit
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectranetics Bridge Occlusion Balloon catheter Recalled by Spectranetics...
The Issue: Possible inability to pass the guidewire through the Bridge device,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Total Hip Application (THA) Product Usage: The Robotic Arm Interactive...
The Issue: Software discrepancy of not showing all the EE constants, when the screen is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Emprint Percutaneous Antenna with Thermosphere Technology Recalled...
The Issue: The firm received consumer reports of the ceramic trocar tip of the Emprint...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Affixus Hip Fracture Nail Recalled by Zimmer Biomet, Inc. Due to During the...
The Issue: During the rework process for the April 17, 2017, field action, it was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.