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. 2,528 recalls have been distributed to South Dakota in the last 12 months.
Showing 5941–5960 of 27,558 recalls
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Design Options¿ / Epidural anesthesia kit (10 count carton) Recalled by B....
The Issue: Kits were assembled with the incorrect Filter Straw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIGENE Clostridium difficile Nucleic Acid Test Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene Enteric Pathogens Nucleic Acid Test (EP) Recalled by Luminex...
The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perifix¿ / Epidural anesthesia kit (10 count carton) Recalled by B. Braun...
The Issue: Kits were assembled with the incorrect Filter Straw.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...
The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Crea Test Card with epoc Host SW v3.37.3 Recalled by Siemens...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM Test Card (BUN & TCO2) Recalled by Siemens Healthcare Diagnostics...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM BUN Test Card with epoc Host SW v3.37.3 Recalled by Siemens...
The Issue: There is potential for discrepant high glucose results in samples with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...
The Issue: Firm has received reports of patient burns in surgical procedures where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Shots were...
The Issue: Shots were terminated by the mAs integrator; however, the 4 ms exposure time...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trexo Device Recalled by Trexo Robotics Holdings Inc. Due to Electrical...
The Issue: Electrical issues that could potentially render the device non-functional,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.