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. 2,516 recalls have been distributed to South Dakota in the last 12 months.
Showing 9241–9260 of 27,558 recalls
Recalled Item: HARMONICHD 1000i Shears (36cm Shaft Length)-indicated for soft tissue...
The Issue: An internal component may be cracked and become lodged behind the energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HARMONIC HD 1000i Shears (20cm Shaft Length)-indicated for soft tissue...
The Issue: An internal component may be cracked and become lodged behind the energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FilmArray Blood Culture Identification (BCID) Panel Product Pouch Label:...
The Issue: Due to product complaints received for false negative results (dropouts)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cordis SABER PTA Balloon Dilation Catheter Recalled by Cordis Corporation...
The Issue: The balloon protective sheath may potentially be contaminated with a foreign...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Recalled by Philips North America LLC Due to Infant/Child...
The Issue: Infant/Child defibrillator pads contain incorrect labeling. This could lead...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Slick Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Murphy Eye Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Endotracheal Tube oral/nasal Magill Recalled by Teleflex Medical...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RUSCH Flexi-Set Cuffed Endotracheal Tube and Stylet Set Recalled by Teleflex...
The Issue: The firm received reports that the endotracheal tube cuff could be inflated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normand Remisol Advance Data Manager Recalled by Beckman Coulter Inc. Due to...
The Issue: There is a potential that the data management system may add additional...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Marque Antibodies Recalled by Cell Marque Corporation Due to Mouse...
The Issue: Mouse Monoclonal Antibody labelled with an incorrect expiry date of 31 Dec...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gastroscope Family # 1-Gastroscopes without a Water Jet Channel Models:...
The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Colonoscope Family # 1-Pentax Video Colonoscopes (EC Family) with One...
The Issue: Updated Reprocessing Instruction For Use (rIFU): Impacted PENTAX Medical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FLASH Ostial System Recalled by Ostial Corporation Due to Angioplasty system...
The Issue: Angioplasty system has a manufacturing issue that has the potential to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew BHR SQUARE HEADED NAIL Recalled by Smith & Nephew Orthopaedics...
The Issue: The nail head may become detached during surgery.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EV3 Pipeline Flex Embolization Device with Flex Shield Technology Recalled...
The Issue: Due to potential push wire fractures in the delivery system during use. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pipeline Flex Embolization Device Recalled by Micro Therapeutics Inc, Due to...
The Issue: Due to potential push wire fractures in the delivery system during use. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Juniper Diagnostic Ultrasound System Recalled by Siemens Medical...
The Issue: Due to intermittent failures of the power supply in the ultrasound system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gore Molding & Occlusion Balloon Catheter Recalled by W. L. Gore &...
The Issue: Complaints received concerning Balloon Catheter leakage from the guidewire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity s System . An automated immunoassay analyzer for Recalled by Abbott...
The Issue: A design defect (hardware and software) allows liquid waste pressure to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.