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. 2,465 recalls have been distributed to South Dakota in the last 12 months.
Showing 15441–15460 of 27,558 recalls
Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 8FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 18FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 12FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 10FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermistor Foley catheter Recalled by Degania Silicone, Ltd. Due to The...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 8FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Maestro 4000 Cardiac Ablation System Recalled by Boston...
The Issue: Reports of unintended continuation of radiofrequency (RF) energy delivery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Tri-Flo Subglottic Suction System Recalled by Vyaire Medical Due to...
The Issue: Vyaire Medical has discovered potential patient safety risk with associated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Espiner Tissue Retrieval System-Eco-Sac Trocar 12mm Vol: 1200 ml...
The Issue: Label was incorrect. The label states that the volume of the retrieval bag...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NICO Shepherd' s Hook - Greenberg Recalled by Nico Corp. Due to Mislabeling
The Issue: Mislabeled hook pouch included a transport/storage label rather than the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: Through investigation, it was determined that H12LP Trocars in scope of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: J-Plasma Precise 360 Recalled by Bovie Medical Corporation Due to There is a...
The Issue: There is a potential risk associated with the PEEK tip of the J-Plasma...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Oasis MRI system Product Usage: Hitachi MR system is Recalled by...
The Issue: The stainless steel belt which runs the length of the table underneath the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.