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. 1,060 recalls have been distributed to South Dakota in the last 12 months.
Showing 9641–9660 of 27,558 recalls
Recalled Item: VIA Microcatheter VIA 21 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical Video Duodenoscope - Product Usage: intended to be Recalled...
The Issue: IFU updated: The warning section of the IFU for both the OE-A63 distal end...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayStation (Treatment Planning System) Model Number RayStation is 6.0.0.24...
The Issue: Evaluation of a clinical goal for the voxelwise worst dose distributions may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VIA Microcatheter VIA 17 - Product Usage: is Recalled by MICROVENTION INC....
The Issue: Due to inadvertently shipping to U.S. customers with international labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Semi-automatic Biopsy-Needle Recalled by INNOVATIVE TOMOGRAPHY PRODUCT GMBH...
The Issue: Sterility Assurance; Coaxial Interventional Needle labeled as sterile may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydrodissection Cannula (Chang) Recalled by Anodyne Surgical Due to The...
The Issue: The product may have a yellowish-brown/greenish-brown residue present at the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multitom RAX with software version VF10 Recalled by Siemens Medical...
The Issue: Siemens identified two issues, In some cases, it is possible to perform an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Logical cup liner - Product Usage: intended to replace a Recalled by...
The Issue: Product mislabeled, with the incorrect product inside the package.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta MOSAIC Oncology Information System versions: 2.62 Recalled by Elekta,...
The Issue: Malware attack
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dialysate Concentrate for Hemodialysis-Liquid/Powd - Product Usage: used in...
The Issue: The lot may have experienced an anomaly during the manufacturing process,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alpha Interlock Suspension System Lanyard Body: An external prosthetic...
The Issue: the firm discovered that, starting on April 1, 2020, a 3/8 dowel pin was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 3 (GTIN 00840682147378) Recalled by GE Healthcare,...
The Issue: The IGS system can experience a single vertical line defect where the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Cardiac Assessment System for Exercise Testing and CardioSoft...
The Issue: If a certain sequence of events occur, the pdf test report that belongs to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Econocare Plus Waffle Overlay- Intended for use as a medical Recalled by...
The Issue: Product contamination-a trace amount of dried bodily fluids may expose...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Change Healthcare Enterprise Viewer - Product Usage: intended to be Recalled...
The Issue: A software defect was identified where the Image Styles defined by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Pneumonia Panel (Penumo) Recalled by BioFire Diagnostics, LLC Due...
The Issue: Elevated rates of false positive/false negative and control failures while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quickslide GramPro 1 Automated Gram Stanier is a microscope slide stainer....
The Issue: Instruments were assembled and serviced using a defective lot of tubing,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13...
The Issue: Malfuncton-Implant did not deploy successfully may necessitate the need for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Critical Care Ventilator Recalled by Draeger Medical, Inc. Due to Three...
The Issue: Three separate and unrelated problems attributed to the software used in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.