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. 2,484 recalls have been distributed to South Dakota in the last 12 months.
Showing 12101–12120 of 27,558 recalls
Recalled Item: VNS Therapy Programmer Recalled by LivaNova USA Inc Due to False positive...
The Issue: False positive warning may occur after: 1) VNS Generator interrogated at 0mA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris PCA Module Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Pump Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal PS Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STEALTH SPRING CLIP 6mm latis (1/4 Force). Non-Sterile Recalled by Applied...
The Issue: Failure of cardiovascular clips to provide sufficient occlusion of the vessel.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Procedure Packs containing AAMI Level 3 surgical gowns Recalled by...
The Issue: The kits contained recalled surgical gowns. The gowns were manufactured at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Presource Procedure Packs containing AAMI Level 3 surgical gowns Recalled by...
The Issue: The kits contained recalled surgical gowns. The gowns were manufactured at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink 2090 Programmer. Used to interrogate and program...
The Issue: Medtronic Conexus Telemetry has been determined to contain two primary cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic CareLink Encore 29901 Programmer. Used to interrogate and program...
The Issue: Medtronic Conexus Telemetry has been determined to contain two primary cyber...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LKT200 Perfusion Circuit Recalled by Organ Recovery Systems, Inc. Due to...
The Issue: Observed leakage at the sample port assembly which could potentially lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Class IV New Era medical laser device Recalled by Inova Lasers LLC Due to...
The Issue: The firm failed to comply with the applicable standards regarding Electronic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ISE Electrolyte (2 X 2L) Reagent Recalled by Beckman Coulter Inc. Due to...
The Issue: Electrolyte reagent, used for clinical laboratory testing to determine CO2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.