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. 2,349 recalls have been distributed to South Dakota in the last 12 months.
Showing 26921–26940 of 27,558 recalls
Recalled Item: Horizon Medical Imaging system. Product Usage: Horizon Medical Imaging is...
The Issue: There is a potential to save reports in RadReport with an Incorrect Final...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Recalled by Carefusion 2200 Inc Due to...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: This voluntary medical device correction is related to Alcon products...
The Issue: This medical device correction is related to Alcon products that present a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo(R) Lab Data Manager and syngo(R) Lab Process Manager Recalled by...
The Issue: When using the syngo Quality Control package the system may not perform as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirLife Isothermal Breathing Circuit Accessory - Infant Patient Y Connector...
The Issue: The Y adapter within the breathing circuit may spontaneously crack, causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IDEV Technologies SUPERA VERITAS Interwoven Self-Expanding Nitinol Stent...
The Issue: There was an error on the outer labeling of this device. The inner label was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Volume Viewer Plus 5.x (Advantage Workstation 4.2) Volume...
The Issue: Incorrect views and measurements possible. GE Healthcare became aware of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit model 8015 Product Usage: The device is Recalled by...
The Issue: The recall was initiated because the Alaris PC unit model 8015 has a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Advantage Workstations Recalled by GE Healthcare, LLC Due to...
The Issue: GE Healthcare is informing you of incorrect measurements when using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Advantage CT/PET Fusion for Advantage Windows Workstation with Volume...
The Issue: GE Healthcare has become aware of a potential safety issue due to incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Seno Advantage 1.x Recalled by GE Healthcare, LLC Due to GE Healthcare...
The Issue: GE Healthcare has become aware of an issue associated with the magnification...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of inaccurate Scale factor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bipolar Forceps model number: S02-XXX Recalled by Stingray Surgical...
The Issue: On 05/23/2012, Stingray Surgical Products, LLC., Boca Raton, FL initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intellispace Portal software. Intellispace Portal is a multimodality thin...
The Issue: Philips is issuing a software update to the Intellispace Portal systems to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra(TM) Jarit(R) Take-Apart Endoscopic Instruments. Integra(TM) Jarit(R)...
The Issue: The Integra(TM) Jarit(R) Take-Apart Laparoscopic Instrument shafts were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LMA Esophageal Intubation Detector (EID) Recalled by LMA North America Inc...
The Issue: The recall was initiated because LMANA has received a complaint that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelliSpace Portal software and Extended Brillance Workspace software...
The Issue: The Intellispace Portal software and Extended Brillance Workspace software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD GeneOhm Cdiff Assay Recalled by Becton Dickinson & Co. Due to Leakage in...
The Issue: Leakage in Cepheid SmartCycler reaction tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYTO-STAT tetraCHROME CD45-FITC/CD4-RD1/CD8-ECD/CD3-PC5 Recalled by Beckman...
The Issue: The recall was initiated because Beckman Coulter has determined that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TetraCXP Software System Recalled by Beckman Coulter Inc. Due to The recall...
The Issue: The recall was initiated because Beckman Coulter has determined that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.