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. 2,373 recalls have been distributed to South Dakota in the last 12 months.
Showing 23001–23020 of 27,558 recalls
Recalled Item: TEGRIS System manufactured by MAQUET GMBH in Germany The Maquet Recalled by...
The Issue: The wrong movement results on the MAGNUS OR table. The button commands on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel 600/800 Access Immunoassay Systems are in vitro diagnostic devices...
The Issue: Beckman Coulter is recalling the Sample Probe Cable because nonconforming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Recalled by Philips Medical Systems, Inc. Due to When a fused series...
The Issue: When a fused series of a sagittal, coronal or radial multi station scan is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products PHYT (Phenytoin) Slides Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics identified a potential for biased results to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 98" (249 cm) Appx 12.3 ml Recalled by ICU Medical, Inc. Due to ICU is...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT 2 Flow Controller Recalled by ICU Medical, Inc. Due to ICU is recalling...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens CentraLink Data Management System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has identified a task scheduler issue with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 83" (211 cm) Appx 10.3 mL Recalled by ICU Medical, Inc. Due to ICU is...
The Issue: ICU is recalling the ConMed Stat 2 flow controller because it may deliver a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ellipse Implantable Cardioverter Defibrillators (ICDs) Recalled by St Jude...
The Issue: An anomaly may result in delayed, partial, or no delivery of high voltage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hitachi Echelon Oval MRI system is a diagnostic imaging device Recalled by...
The Issue: The Gradient Coil was found to have a failure mode that allowed it to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco The Monaco system is used to make treatment plans Recalled by Elekta,...
The Issue: Incorrect Delivery of Composite VMAT Fields - When DICOM is exporting an arc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FOCAL Sim Workstation Recalled by Elekta, Inc. Due to When DICOM is...
The Issue: When DICOM is exporting an arc plan (VMAT, Dynamic Conformal of 3D Static...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4D Integrated Treatment Console (4DITC) Recalled by Varian Medical Systems,...
The Issue: Due to user error, the 4DITC can improperly allow users to clear a safety...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Dimension Vista¿ CHEM 1 CAL Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has received complaints for low recovery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below...
The Issue: Potential issues with the ProVue driver have been identified which may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Array LaserLink Recalled by Lumenis, Inc. Due to Lumenis initiated a...
The Issue: Lumenis initiated a field-correction for the Array Laser Link",...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Scorpio femoral component. Howmedica Osteonics Corp....
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Orthopaedics Triathlon femoral component. Howmedica Osteonics Corp....
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Howmedica Osteonics RESTORATION Acetabular Augment System Recalled...
The Issue: The peel strength of the inner blister may have been below internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.