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. 2,365 recalls have been distributed to South Dakota in the last 12 months.
Showing 23841–23860 of 27,558 recalls
Recalled Item: The Centricity PACS Workstation is intended for use as a Recalled by GE...
The Issue: It has been identified that in a reject image workflow where multiple...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics v9.5 system. A Picture Archiving and Communication System...
The Issue: Systems with the affected serial number are experiencing a software error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iLab Ultrasound Imaging System Recalled by Boston Scientific Corporation Due...
The Issue: Specific iLab Ultrasound Imaging Systems using newest 3.0 (Polaris 1.0)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Imaging XS Syngo Imaging XS is a Picture Archiving Recalled by Siemens...
The Issue: A complaint reported that the archiving method at one customer site was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMIA v1.0 APD System. For Automated Peritoneal Dialysis (APD) therapy...
The Issue: Additional warning in the AMIA APD System labeling for patients vulnerable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor with system software version...
The Issue: Software communication failure may occur on the HeartStart XL+ locking the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ACUSON X700 Ultrasound Systems with software version 1.0.00 Recalled...
The Issue: When fourSight 4D ultrasound imaging, 3-Scrape real time 3D imaging, or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABACUS TPN Calculation Software Recalled by Baxter Corporation Englewood Due...
The Issue: 1. ABACUS v3.1 may calculate quantities of electrolytes that are double the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Potential safety issue...
The Issue: Potential safety issue with gradient coil electromechanical connections...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Circular Lock Screws Recalled by Genesys Orthopedics Systems, LLC Due to The...
The Issue: The recall is being initiated because MK Precision (the Circular Lock Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRABECULAR METAL MODULAR ACETABULAR SYSTEM Recalled by Zimmer, Inc. Due to...
The Issue: The shell was missing the locking ring.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Medical Systems Computed Tomography X-ray systems (Brilliance CT...
The Issue: A customer reported that the table top had become free floating. A Field...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alligator Retrieval Device (ARD). Used in the peripheral and...
The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 550 TxT Treatment Table of the Digital Linear Accelerator (LINAC) Recalled...
The Issue: Table may lose calibration during patient treatment, which may cause the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PS-C Femoral Nonporous Rt Sz 6 Recalled by Ortho Development Corporation Due...
The Issue: A femoral component containing pegs was found in a box for the pegless version.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pipeline Embolization Device (PED). Used endovascular treatment of adults...
The Issue: Potential for the PTFE (polytetrafluoroethylene) coating to delaminate and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Linear Accelerator (LINAC) models. Product Usage: deliver X-ray...
The Issue: Siemens Radiation Oncology became aware that customers may be using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EZ-IO 45mm (40kg & up) Needle Set Recalled by Vidacare Corporation Due to...
The Issue: The voluntary recall is due to the needle set not meeting its specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Henora 300psi I.V. Catheter Extension Set Product Usage: Recalled by RGI...
The Issue: Problem with low adhesion of the tubing to luer connection which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GLOBAL¿ Anchor Peg Glenoid Plus (APG+) 2.5MM Breakaway Guide Pin Recalled by...
The Issue: Urgent Device Correction notifications are being sent to USA distributors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.