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. 2,373 recalls have been distributed to South Dakota in the last 12 months.
Showing 23301–23320 of 27,558 recalls
Recalled Item: RUSH81 Prosthetic Foot Product Usage: Prosthetic foot for human use Recalled...
The Issue: Ability Dynamics is recalling RUSH81 Prosthetic Foot because the existing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SUTUREFIX Ultra S with 1 #2 Ultrabraid (blue) Product Code: Recalled by...
The Issue: Sterility of device is compromised due to breach in sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare ADVIA Acid/Base Reagent 1 and 2 Kit containing Recalled...
The Issue: Swollen acid bottles due to a trace metal contamination in the Acid Reagent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Systems TnI-Ultra assay Recalled by Siemens Healthcare...
The Issue: The solid phase reagent in some of the ADVIA Centaur¿ TnI -Ultra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage BNP Calibrators for the Beckman Coulter Access Family Recalled...
The Issue: Alere San Diego is recalling Alere Triage BNP Calibrators for the Beckman...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable laparoscopic instruments are packaged as non-sterile. Cleaning and...
The Issue: Additional caution statements have been added to the Instructions For Use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KODAK DirectView DR 9000 System Recalled by Carestream Health Inc. Due to A...
The Issue: A control system failure may cause the U-Arm to move downward unexpectedly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iGUIDE System Product Usage: The intended use of the device Recalled by...
The Issue: A bug in the software prevents the iGUIDE software from logging off.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tytin Regular Set Recalled by Kerr Corporation Due to Kerr Corporation is...
The Issue: Kerr Corporation is recalling one (1) lot of Tytin Regular Set ( Part Number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Guide Blocks for the 2 Column Plate 6 Hole Recalled by Synthes, Inc....
The Issue: The Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOSAIQ MOSAIQ is an oncology information system used to manage Recalled by...
The Issue: MOSAIQ does not re-calculate the agent volume when the user changes the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.