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. 2,330 recalls have been distributed to South Dakota in the last 12 months.
Showing 33941–33960 of 47,632 recalls
Recalled Item: RadSuite Recalled by Merge Healthcare, Inc. Due to Potential incorrect...
The Issue: Potential incorrect Standardized Uptake Values (SUV) measurements in RadSuite.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView are gamma cameras Recalled by Philips Medical Systems (Cleveland)...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView XCT & BrightView XCT Upgrade Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC Recalled by...
The Issue: Devices reported to have a smooth texture to the outer surface of the metal,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightView X are gamma cameras Recalled by Philips Medical Systems...
The Issue: The firm discovered four issues with the BrightView Family systems. Issue 1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...
The Issue: There were two potential interference conditions identified with the way the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...
The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...
The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...
The Issue: On a rare occasion, there is a potential to assign a patient result to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...
The Issue: An issue with the Panorama Central Station may cause the system to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...
The Issue: The door latch may not fully close and the door may open unexpectedly. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lindane Lotion Recalled by Morton Grove Pharmaceuticals, Inc. Due to...
The Issue: Super-Potent Drug: Out of Specification Assay test results were reported for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Asset BOLD Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oasis Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Formula Capsules Recalled by Bee Extremely Amazed LLC Due to...
The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.