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. 2,386 recalls have been distributed to South Dakota in the last 12 months.
Showing 20441–20460 of 47,632 recalls
Recalled Item: Endotrac ECTR Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Triangle Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Push Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endintrak 2 Hook Blade Recalled by Stryker GmbH Due to The seal integrity of...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrac EPF/EGR Hook Blade Recalled by Stryker GmbH Due to The seal...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endotrig ETF Hook Blade Recalled by Stryker GmbH Due to The seal integrity...
The Issue: The seal integrity of the sterile bag containing the kits may be compromised.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Randox Urinalysis Control Level 2 (IVD) - Product Recalled by Randox...
The Issue: Analyte range for Leukocytes for use with the Siemens Multistix method is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implant BioCell Round Moderate...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle Recalled by Allergan PLC Due to The action was initiated following...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle133 Plus Tissue Expander With/Without Suture Tabs Recalled by...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Komuro Recalled by Allergan PLC Due to The action was initiated following...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 150 Full Height and Short Height Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan 410 TruForm 2 (Soft Touch) BIOCELL breast implant...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle Inspira Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle and McGhan Silicone-Filled Breast Implants Recalled by Allergan PLC...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: McGhan Croissant-Shaped Tissue Expanders Recalled by Allergan PLC Due to The...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders w/Suture Tabs BIOCELL Full Height Variable...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 133 Tissue Expanders (also named style 133 BIOSPAN Tissue Recalled...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 410 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natrelle 510 Recalled by Allergan PLC Due to The action was initiated...
The Issue: The action was initiated following notification by the U.S. FDA of their...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.